WE WORK WITH OUR TRAINING PROVIDER PARTNERS TO BRING THE EXCLUSIVE HANDPICKED TRAINING PROGRAMS PACKED AS PER CUSTOMERS REQUEST & FEEDBACK

12 Essential Sessions on Tax Laws: What You Must Know About the Tax to Stay in Compliance

Learn everything you need to know about and related to Tax laws. These sessions will contain information from basic laws of tax, garnishments and payroll to the new updates in the areas and also you will learn about complying with federal and other government agencies. As well as all the reporting requirements and forms you need information on are gathered in this set of trainings.

20 Set of Informative Courses to Learn All About Excel and Its Advanced Techniques

This knowledgeable pack of training will make you gain knowledge on various forms of Excel and gain an understanding of multiple techniques that are used and in trend with Advanced Excel spreadsheets and dashboards. Also, you will learn tips & tricks on how to use Microsoft Excel in different industries along with advanced formulas, steps to analyze data, and the benefits of using Excel as well.

19 Training Courses to Get to Know the Best Practices in the Pharmaceutical Industry

This set of course is designed to provide you with an understanding of the multiple areas within the Pharmaceutical industry. You will get information about the requirements and best practices for the Pharma Industry which will include Effective Pharma Technology Transfer, Implementation of Pharma management system, manufacturing, Advertising and marketing of products, Inspection and safety guideline and so on.

Best Practices for Medical Device Industry: An Exclusive Set of 16 Webinars

These sets of training will help you get familiar with various areas of the medical device industry. This will contain how to minimize risks by applying practical strategies to comply with the currently applicable, relevant laws and regulations governing medical devices, further streamlining the regulatory process using case studies and examples.

Pack of 16 Best Seller Webinars on All FDA Related Regulations and Requirements

These set of courses are intended to provide you with all the FDA related regulations, compliance and requirements. Critical issues will be discussed so you can develop and maintain effective and efficient compliance. These topics will cover legal requirements which will include FDA auditing, investigations, social media marketing, SOPs, TMS, 501(k) requirements, import and export requirements, Spreadsheet and electronic record maintenance and much more.

7 Essential pieces of training for Biotechnology Industry

This set of courses provides you with wide variety of areas in the Biotechnology industry including Sterile Product Manufacturing & Testing, Contamination control, risk within the manufacturing process and also auditing for potential sources of contamination. Also guide you with best methods to detect and mitigate any issue which poses a threat.

A Set of 4 Programs to Ensure Compliance with CMS

This set of training programs is designed to Ensure Compliance with the CMS. You will be learning what are the CMS proposed changes are in recent years, infection control issues from CMS, Sunshine Act and CMS Emergency Preparedness Rule for Medicare and Medicaid Providers and Suppliers and much more.

6 Best Training Courses on Cleanrooms: How to Maintain and Control Contamination/Disinfection

This webinar will provide valuable guidance on how to maintain cleanrooms and all the related regulations, techniques and operations related to it. And also will guide you about various strategies to avoid risks and implication for cleanrooms.

6 Top-Rated Courses on Leadership & Team Management

These set of training programs are designed to learn all about leadership skills, Team management, Communication and various areas related to Organizational Development. Make the best use of all the programs presented by the Speaker “Christopher DeVany” on these mentioned topics to improve personal skills as well as your team performance.

9 Exclusive Webinars on Pharmaceutical Organizations Standards and Requirements

This package training program helps the participants to learn about QMS that are common to the pharma and medical devices and how to implement QMS in one umbrella, learn about the proposed changes to USP 797 and 795 rules for compounding for individual patients as well as ‘for office use’ compounding, and more. How to master a standardized approach to technology transfer projects. Join this training to learn the best practices for effective pharma technology transfer. Learn to review new materials in the GS1 US guideline and help you prepare to comply with the 2023 requirements, learn more about AE, SAE, AR and SUSAR, reporting timelines, sources of information, preclinical, clinical and post marketing, and more, learn the regulations pertaining to objectionable microorganisms and the methods to control and reduce the amount of objectionable microorganisms. Attend this trending webinar to learn about principles of Total Organic Carbon Analysis, analytical approaches in different instruments, setting limits based on TOC and get trained on importance of quality in Compressed Air, Pharmaceutical Compressed Air System Design, Contamination Prevention, GMP Testing Standards and more.

12 Fundamental Courses on Clinical Trials – Principles and Best Practices

Get trained on these package training phases of clinical research, Good Clinical Practices, elements of a quality system, ethics in clinical trials and more. Attend this training on clinical supplies and learn what are the steps required for labeling and packaging the supplies for use in a clinical trial, learn the differences between device and drug clinical research and the latest regulations governing the use of drugs and devices in a clinical research, learn how to apply Computer System Validation and System Development Life Cycle Methodologies to computer system validation in support of clinical trial work. Participants will understand the key components of a QMS, key elements of a document management program, critical aspects of a training program, how to prepare clinical site staff for internal and external audits, discuss best practices for an internal audit program. In one of the training programs Dr. Mukesh Kumar shares tips for addressing potential issues related to using social media in the current clinical research landscape. This package will provide practical tips for using social media to approach, educate and recruit clinical trial participants. Sign up to know the clinical evolution, and guidelines of MEDDEV 2.12-2 on post market clinical follow-up and also get trained on the new Regulation EU No 536/2014 and its effects.

12 Fundamental Courses on Clinical Trials – Principles and Best Practices

Get trained on these package training phases of clinical research, Good Clinical Practices, elements of a quality system, ethics in clinical trials and more. Attend this training on clinical supplies and learn what are the steps required for labeling and packaging the supplies for use in a clinical trial, learn the differences between device and drug clinical research and the latest regulations governing the use of drugs and devices in a clinical research, learn how to apply Computer System Validation and System Development Life Cycle Methodologies to computer system validation in support of clinical trial work. Participants will understand the key components of a QMS, key elements of a document management program, critical aspects of a training program, how to prepare clinical site staff for internal and external audits, discuss best practices for an internal audit program. In one of the training programs Dr. Mukesh Kumar shares tips for addressing potential issues related to using social media in the current clinical research landscape. This package will provide practical tips for using social media to approach, educate and recruit clinical trial participants. Sign up to know the clinical evolution, and guidelines of MEDDEV 2.12-2 on post market clinical follow-up and also get trained on the new Regulation EU No 536/2014 and its effects.

Pack of 11 Comprehensive Training on FDA Rules and Regulations for Medical Devices

This package training program will cite what are the key considerations in medical device design and validation that can help prevent FDA 483s, poor due diligence can lead to issues like recalls or warning letters. Attend this training to understand FDA Expectations for Purchasing Controls, lessons learned from quality issues, developing effective purchasing controls, more. This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices, an overview of Medical Device Registration and Approval Process for the Pacific Rim (including China, Singapore, Taiwan and Hong Kong). A guidebook for knowing the regulatory and compliance requirements in auditing subcontractors for Pharma and Medical Device. Get informed on the next revision of ISO 1385:2006 standards and the changes, requirements that Medical Device Companies has to make. Learn IQ, OQ, PQ methodologies for validating Medical Device Software; learn everything about Quality Management System that is common in Pharma and medical device. Get a thorough knowledge on Complaint Management and Medical Device Reporting in FDA for maintaining public safety. Register for this webcast and Medical Device Companies get trained on software FMEA, its applications to get rid of the failures, mishaps that happen in the Medical Device Design and Development Process. Get trained on the Medical Device Registration and Approval Process for South America.

10 Interactive Training Programs Every HR Professionals Needs to Do to Succeed

This comprehensive training package deal with various roles and responsibilities of the HR. Participants will understand how to effectively import data from various sources, how to get data in the right shape to optimize the Excel tool set and more, practical techniques to help you get things done in today’s chaotic and constantly changing work environment. Are you responsible for hiring new resources to your organization? Join this training to learn the hiring best practices. Gain an understanding of key HR metrics and identify and assess its strategic and operational impact. Outline the record retention and notification requirements for several federal laws and employers know how long to keep or destroy employee records and documents. How to communicate more assertively and effectively? A must attend training program for Executives, Managers and HR Professionals. Learn the current trends and critical components in HR auditing by attending this interactive training program by HR expert Ronald Adler. This training program will help you gain an understanding of key HR metrics and identify and assess the strategic, tactical and operational impact of HR Metrics. Learn how to align performance management with organizational goals and understand what the Five Functions of a Team are. Learn how and why HR sets the tone for customer service and how to ensure that HR is correctly defining the service culture for organization’s valuable internal customers.

10 Best Selling Webinars on Everything You Need To Know About Managers for Effective Team Handling

This package training program is about how to be a successful person in both workplace and personal life. Get tips on managing and maintaining healthy workplace culture. Participants can Boost up their skills in Customer Relationship Management and Interaction with customer matters. This training will enhance your skills with Project Management; learn the best 8 keys to bring your every project on time and on budget, learn the best practices of Project Management to complete your work with perfection, learn the essentials and best practices of Project Management to complete your work on dot. Do you wish to improve your negotiation effectiveness immediately? Attend this package program and learn to develop an effective negotiation plan and strategy, learn tips and tricks of time and task management and understand the value of working smart and also learn the key communication skills, important constructive feedback guidelines, and more. Participants learn how to fine-tune off-site management skills in an environment where you don’t have to worry about making a costly mistake. Learn what you need to be able to deliver better and more effective results-oriented presentations. Join this audio conference by Chris DeVany in this interactive package training program to understand how to unleash the power of accountable communication and to boost productivity.

Step by Step HIPAA Rules and Audit Practices: 7 Trending Courses on HIPAA Compliance

This package training will walk the attendee through 3 Step HIPAA safe harbors that focus on HIPAA Rules for transmitting informational email and text messages to patients, which HIPAA law applies to Business Associates and the 5 steps needed for full HIPAA compliance. Attendees will also get o understand what are the HIPAA Rules in action – steps that are blueprint to prevent, prepare for, respond to and recover from a Ransomware Attack, how to handle HIPAA security incidents, breaches, and complaints and the Department of Health and Human Resources Investigations, the best practices to maintain compliance with HIPAA, what are the penalties for violating the rules and how to handle a HIPAA audit, the 5 steps of HIPAA breach notification rule requirements of covered entities and business associates. Apart from these points the webinar will also cover key areas including development and execution of a manageable auditing and monitoring plan relating to HIPAA compliance targeting common high risk issues, the common social media risks from a HIPAA compliance perspective and how to learn what a HIPAA security incident is and elements you need to have in your security incident report and response policy and procedure.

9 Vital Courses on FDA Regulation: 21 CFR Part-11, 510(k), Excel Spreadsheet Validation, GMP Guidelines, Compliance and Custom’s Requirements

This comprehensive training package will discuss the regulatory perspective on promoting off-label uses for manufacturers, essential elements of a TMF for clinical trials, activities of set-up, maintenance, and monitoring will be discussed using case studies to highlight common deficiencies and potential solutions. Package highlights key elements of rules governing HCT/Ps using case studies, learn the methods to plan and execute Excel Spreadsheet Validations that satisfy FDA Requirements and know more about FDA guidance on Mobile Medical Apps., uses. This training is intended to discuss the recent changes, hurdles, and requirements for premarket notification [510(k)] compliant with eCopy and Refuse to Accept Policy (RTA) requirements, learn how to develop a standard approach to testing for all computer system efforts regulated by FDA that will be robust and will meet all compliance requirements, get guidelines and practical insights on 21 CFR Part 11 namely Electronic Records and Electronic Signatures and also know the best practices to implement these in a regulated environment.

Pack of 6 Powerful Training Courses Every Manager Must Attend and Adopt and Implement

This package training program is about how to be a successful person in both workplace and personal life. Get tips on managing and maintaining healthy workplace culture. Participants learn how to fine-tune off-site management skills in an environment where you don’t have to worry about making a costly mistake. Learn what do you need to be able to deliver better and more effective, results-oriented presentations. Join this audio conference by Chris DeVany in this interactive webinar to understand how to unleash the power of accountable communication and to boost productivity. This presentation gives you practical techniques for controlling time and also the steps to build a high performance team in 90 days.

5 Courses on Exporting to Mexico, Mexican Import Process, Mexican Customs and INCOTERMS Common Practices with HTS

Harmonized codes (or tariffs) are an international customs classification system now used by most trading nations throughout the world. Get a chance to learn the new sets of amendments recommended by the World Customs Organization to the Harmonized Tariff Schedule effective January 1, 2017. Learn about Mexican Import process from Linda B Sarabia, who is a Mexican Customs and foreign trade consultant since 1991. In Exporting to Mexico Webinar Series 1- Learn how the Import Process works in Mexico, Who can import to Mexico, Role of customs broker. In Exporting to Mexico Webinar Series 2 learn about Mexico import and export HTS codes, non-tariff barriers compliance, and documentation compliance. The Exporting to Mexico Webinar Series 3 explains what INCOTERM is? Mexican customs criteria on INCOTERMS? Which INCOTERMS is apt when exporting to Mexico?

Organizational Strategies for Reducing Human Error in GMP Environments: 4 Informative Webinars

This advanced package training course helps you understand the importance of reducing human errors in GMP related environments and the need for CAPA effectiveness. This program will help executives to recognize the importance of writing procedures to avoid human errors and best formats and content elements for SOPs. Expert speaker Ginette M Collazo also talks about factors and causes of human errors in GMP related environments and provides practical tools for controlling human error in the manufacturing floor.

Overcoming the BSA/AML Challenges-6 Webinars Every BSA/AML Personnel must Attend

The Bank Secrecy Act (BSA) was passed by the United States Congress in 1970. Bank Secrecy Act requires U.S. financial institutions to collaborate with the U.S. government in cases of suspected money laundering and fraud. Financial institutions must be compliant with BSA rules and regulations. A comprehensive and compliant BSA/AML program helps a financial institution to conduct risk assessments in order to identify BSA/AML risks that could impact the financial institution and implement controls to mitigate these identified risks. This 6 in one package training program will help you obtain guidance on doing business with marijuana customers; learn what are the revisions to the BSA AML examination model and how to ensure your organization has prepared them; get an overview of the importance of the risk based approach; AML/OFAC risk assessment best practices; and get guided on the new FinCEN SAR.

Be up-to-date with GMP Guidelines: 7 Interactive courses by Industry Experts

The FDA’s regulations on Current Good Manufacturing Practices (cGMP) affect many different phases of pharmaceutical, biologic and biopharmaceutical development. Good Manufacturing Practices (GMP) are a set of measures that aim to provide guidance for manufacturing, testing, and quality assurance in order to ensure that drug products are safe for human consumption. This Package training course is suitable for everyone who needs to be up-to-date with the GMP guidelines. This package of seven webinars contains beautifully designed, interactive presentations that will allow you to enjoy the learning process and easily understand the fundamentals of Good Manufacturing Practice.

Trade Compliance-5 Courses on US Export and Import Requirements

Get the information you need to stay compliant with customs regulations by buying this package training. Learn what are the FDA Import and Export Requirements, how to protect your intellectual property abroad, documentation and procedures to be followed by exporters and importers while trading in Mexico, how to increase the compliance and efficiency of clearing your imports, and how to implement third party logistics (3PL) to outsource your logistics.

6 Useful Webinars on Clinical Trial Protocols, SOPs for Clinical Sites, Trial Master Files, Sunshine Act and GCP

This package training will walk the attendee through 10 critical steps in the development of a clinical protocol, which SOPs should be implemented and what methods should be used to develop and document FDA-acceptable conduct of clinical sites activities, essential elements of a TMF for clinical trials, the Sunshine Act, critical elements of Good Clinical Practice (GCP), and how to manage Protocol Deviations and Violations.

Credit-Loan Management-7 Vital Webinars for Loan Officers and Credit Analysts

Imagine finding yourself suddenly in a senior credit administration position at your bank due to required personnel changes as a result of frequent credit losses; Or, your bank’s credit administration seems disconnected, un-organized and free flowing and lacks effective management oversight; Or you are in a lending position and the credit administration function at your bank fails to provide structure, guidance and leadership. If any of these scenarios point to you or your financial institution, this package course will address the factors you need to know to make a positive difference in the credit administration at your bank.

Pack of 5 Best Selling Webinars on Medical Devices

This webinar package will help you understand the FDA device regulations related to Excel spreadsheets; best practices in preparing metrics and dashboards for management review; how to improve your root cause analysis leading to real and lasting improvements and how to use risk analysis tool on software design. The package will also give insights on FDA guidance on Mobile Medical Apps.

HR Compliance-Learn Roles and Responsibilities of HR with 7 courses

This comprehensive training package deals with various roles and responsibilities of the HR including LGBT Rights, bullying versus harassment laws, managing employee terminations and exits, recognizing and handling dysfunctional employees, understanding the meaning of exempt employee, HR Recordkeeping requirements, building a salary compensation system.

Credit Loan Management-5 Exclusive Webinars

This training package will provide the “big” picture of credit, how to work with the account to collect from them effectively and still retain them as an account; teach skills required to write an effective credit memorandum; make you understand how to calculate and interpret cash flow is essential for successful bankers; show how you can forecast your monthly cash flow within 95% or better; and also help you understand both the importance and limitations of financial projections.

4 Training Courses on How to Manage FDA 483s and Warning Letters

When the FDA documents that a firm has significant deviations from applicable legal requirements, it will issue that firm a Warning Letter. As an enforcement tool, the FDA Warning Letter tells you that your firm is facing harsh enforcement action unless you correct the errors of your ways. What you say and, more importantly, what you do can make or break your future with the FDA. The Warning Letter is a regulatory spring board that leads you into treacherous waters. Currently, the FDA aggressively manages Warning Letters. The threat of further legal action is real. You have little, if any, breathing room for mistakes or oversights in your response. By effectively managing your Warning Letter response, you can avoid being a statistic for other legal actions, like seizure, injunction, prosecutions, fines and product detention.

7 Computer System Validation Courses for Life Science Industry

The basic concepts of computerized system validation originated in the 1960s, with the Department of Defense and NASA. Validation of systems became a growing issue within the pharmaceutical industry during the late 1980s and early 1990s, as the use of computerized technologies became commonplace in the research and manufacturing of drug products. The FDA issued a series of regulations and guidelines to define regulatory expectations for computerized system validation. In today’s environment, virtually all aspects of research and manufacturing are conducted using computerized systems, yet the planning, conduct, and necessary controls for validation of these systems remains problematic for many companies and industry professionals.

Need Guidance for Auditing? Here are 4 Webinars for Audit Success

This package training has been specifically designed to help attendees prepare for FDA and EU inspections. It will provide a background and understanding of the role played by the regulatory inspectors, and the administrative and enforcement powers. Attendees will be walked through the key stages of FDA and EU inspection processes and understands the various types of inspections that can be carried out. These presentations will also help you to learn why audit interviews are important and what it means for auditors to be fair during an interview, and most importantly how to maintain a good Design History File (DHF) that will help a manufacturer in a regulatory compliance audit.

5 Top Ranking Webinars on Principles of Lean Documents and Lean Configuration

This webinar package presents a new approach based on solid principles and proven practices. Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements as design inputs. These design inputs then form the basis of the design specification, which becomes the design output. Since design controls require tracing backwards and forwards in order to link the requirements to their satisfaction, a problem faced by many companies is in having to maintain duplicate information across many controlled documents. Prior to computer systems and databases, managers and quality personnel created complex visual numbering systems and separate files for purposes of retrieval and control. These grew over the years into the extremely complex and convoluted systems we find today throughout the life sciences. In this Lean Documents and Document Control training we learn the different types of lean documents and the usage of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents, pros and cons of lean vs. non-lean documents. This webinar series will also present a fresh new approach on applying lean principles to instituting corrective and preventive actions.

3 Must Buy Webinars on Product Stability Testing, Gas Testing and Water Testing Program

This package training will explain in detail, the requirements of the FDA’s drug stability guidelines that are stipulated for drug products and how to design a product stability testing plan that can be applied to new or modified products in the pharmaceutical, biotechnology and medical device industries. It will also provide a great resource to manufacturers and gas suppliers/vendors who are planning a new, existing or modifying an existing gas system so as to meet the requirements of ISO 8573, USP or FDA requirements. Apart from giving insights on pharmaceutical product test and gas testing, this webinar will help the attendee gain an understanding of the requirements of Pharmaceutical Water Systems per current USP <1231> Water for Pharmaceutical Purposes.

5 Webinars covering BSA/AML Audit Best Practices, Risk Management

The United States Congress passed the Bank Secrecy Act (BSA) in 1970. Bank Secrecy Act requires U.S. financial institutions to collaborate with the U.S. government in cases of suspected money laundering and fraud. Financial institutions are required to be compliant with BSA rules and regulations. A comprehensive and compliant BSA/AML program helps a financial institution to conduct risk assessments in order to identify BSA/AML risks that could impact the financial institution and implement controls to mitigate these identified risks.

5 Excellent Crash Courses on varied Features of Microsoft Excel

Microsoft Excel is not a mere spreadsheet application to create reports. Excel offers a variety of hidden features such as macro recorder that can streamline repetitive tasks. Excel also helps minimize both data integrity risks and spreadsheet maintenance. It will also help you discover the nuance in Excel where the wrong choice of workbook format can disable key features. This package training course will also help you to learn alternatives to manually copying and pasting data that you can manually compile into reports, summaries, and charts. Other key areas covered in this package training course are: Excel’s Data Validation feature, VLOOKUP function, Worksheet and Workbook protection, Excel’s Very Hidden worksheet feature, Excel’s Trace Dependents and Trace Precedents features, cell comments, range names, INDIRECT and FORMULATEXT functions, Evaluate Formulas feature and Watch Window feature.

2 Info-Packed Webinars on Computer Compliance & Cloud Impact

Cloud based software as a Service (SaaS) applications and Cloud services have transformed into major players in the IT marketplace serving life science regulated industries such as Good Practices in Clinical (GCP), Laboratory (GLP), and Manufacturing (GMP) or GXP. Software as a Service (SaaS) uses cloud computing for delivering a single application to multiple users, regardless of their location, rather than the traditional model of one application per desktop. It permits to manage activities from central locations in a one-to-many model, including pricing and management characteristics.

3 Solid Training Materials on Workplace Retaliation and Investigation

No employer will demote, fire, retaliate against an employee for filing a complaint on discrimination, taking part in a discrimination proceeding, or opposing discrimination. The laws that forbid discrimination on the basis of color, race, religion, sex, gender and disability also prohibit retaliation against persons who go up against unlawful discrimination or take part in an employment discrimination proceeding. When employees raise a complaint regarding discrimination or work place harassment, it is imperative that an employer must take it seriously and implement a resolution step. Federal law requires employers who know of possible harassment or retaliation to investigate. The investigator appointed must have the capacity to analyze and compile data gathered during the process of investigation in an organized manner.

3 Power Packed Webinars Essential for EHS Management

This EHS webinar package will teach you more on the levels of Environmental, Health and Safety (EHS) management. In addition, it would widen your knowledge base associated with the management of day to day environmental requirements and operations.

3 Sort-after Webinars on Design Control Guidance and IVDs for Medical Devices

The FDA has identified design control as a focal point in its inspectional approach to compliance. The Quality System Regulation 21 CFR Part 820 includes requirements for design controls. The regulation requires design validation to ensure your design or design changes will meet both defined user needs as well as your defined intended uses.

Combo Pack of 5 Best Webinars on “Medical Device Reporting”

Medical Device Reporting is the means by which adverse events and malfunctions with medical devices are reported to the FDA. Under the Safe Medical Devices Act of 1990, device manufacturers, importers and user facilities must report known device-related deaths to the FDA.

6 Webinar Series on Quality Management System and Internal Auditing for Devices

Effective quality management systems are identified as a pivotal regulatory factor for allowing medical device manufacturers to market their products around the world. ISO 13485 is a quality management system standard particularly for the medical device industry, which encircles key aspects plus additional industry-specific medical device essentials.

7 Power Packed Webinars on Employee-Organization Relationship and Effective Employee Management

The Employee-Organization Relationship (EOR) has increasingly become a polestar for researchers in organizational behavior, human resource management, and industrial relations. Even the best organizations periodically make mistakes in dealing with employees. They mess up their opportunity to create effective, successful, positive employee relations. Research shows that employees who are motivated, appreciated, and aligned produce measurably better business results.

5 Essential Courses on Principles and Practice on Clinical Trials

OnlineCompliancePanel has complied 5 essential courses in clinical trial and clinical research. These webinar trainings cover various aspects of a clinical protocol from initial synopsis to various elements of the protocol, role of various personnel in finalizing the protocol, and troubleshooting common issues. The basic elements of a clinical trial protocol, the dos and don’ts of clinical trial procedures, development of a new protocol, amending protocols, scientific and ethical review of clinical protocols will be discussed. Also discussed will be role of interactions with the FDA, global clinical trials, and projected trends for the near future.

6 Webinars for Employers on Types of Employee Fraud and Mitigation Steps

Many organizations don’t think about the fraud issue until something has been identified and they need someone to perform and investigate. Inherently, organizations strive to ensure the individuals they hire are honest and ethical. Accounts Payable (AP) is the one business function that, in many organizations, is more vulnerable to fraud than any other. That is because all funds that flow out of the organization must first pass through AP. And over time, dishonest insiders and vendors have created newer and craftier methods of stealing from organizations by exploiting control weaknesses in the AP function. Listed below is some of the top Account Payable: Fraud detection and prevention programs, which would enable you to quickly recognize the red flags of AP fraud in your organization and financial records. These programs will also assist you in providing cost-effective anti-fraud controls to protect against the growing army of fraudsters both inside and outside their organizations.

4 Must Learn Webinars on US Federal Tax Forms and Most Popular IRS Forms & Pubs

The following training is a pack of most informative training materials on topics related to United States most Popular IRS Forms & Pubs. The training materials cover top aspects for a taxpayers and tax-exempt organizations to report financial information to the Internal Revenue Service (IRS) of the United States. These courses provide understanding on how United States Internal Revenue Service applies to organizations pursuant to information like Form W-2, Form W-4, Form W-9, 1099-MISC (2014), Form 8938, Forms 941, FATCA Act, CP-2100 Notice, Penalty notices (972-CGs), IRS TIN Matching, IRC Section 132 and beyond, etc.

5 Webinar Series on Lyophilization

This webinar package will cover optimized, scientifically based lyophilization cycle development for pharmaceutical, diagnostic, and food products. It will untangle the thermal properties of products, how they influence freeze-drying, and the analytical techniques used to determine these.

5 Significant Training courses on ‘SOP’ Management

SOP (Standard Operating Procedure), is used in a variety of different contexts, including healthcare, aviation, engineering, education, clinical research and many more. This webinar series will edify you in creation, management and implementation of adequate SOPs according to FDA criterions.

7 Courses on FDA Inspections and FDA Audits

FDA compliance is one of the most vital subjects for any organization as, without it, their credentials will certainly be called into question. This comprehensive webinar series will prioritize FDA standards and best practices that apply to all industries in the life science scope.

3 Vital Courses on FDA 21 CFR Part-11: Concept, Compliance and Auditing

Title 21 CFR Part 11 of Food and Drug Administration (FDA) guidelines on electronic records and electronic signatures. Part 11, as it is frequently called, elucidates the parameters under which electronic records and electronic signatures are considered to be authentic and equivalent to paper records. The solution to FDA 21 CFR Part 11 compliance is to utilize the law to your benefit, and not tries to ignore it or evade it.