Top Pharmaceutical and Medical Device Trainings in 2023
Complaint Handling Requirements
Mar 21 This 90-minute accredited course is intended to help you better understand and get familiar with the requirements for complaint files and key requirements
Medical Device Process Validation Training for Professionals
Mar 22 This 90-minute session on risk-based verification and validation planning will discuss "must have" elements from the U.S. FDA cGMP, EU MDR, ICH Q9 and ISO 14971
How to write SOP's that Avoid Human Error
Mar 28 This Webinar will discuss the primary cause of quality and production losses in many industries
Conducting Successful Quality Audits: Best Practices for Managing Inspection Situations
Apr 04 In this 90-minute accredited training, you will learn the importance of having a good supplier audit program and how to develop one that is robust.
Master the Vendor Auditing of your Computer Systems Regulated by FDA
Apr 05 This webinar will provide the best industry practices to follow when auditing a vendor of a computer system
US FDA Labeling Requirements for Medical Devices
Apr 11 In this webinar, including some little known or controlled areas which are subject to regulatory scruinty
Excel Spreadsheets - Develop and Validate to Eliminate 483s
Apr 11 This session will make you a better Excel user, saving you time and costs
FDA Case Scenarios: Best Practices for Managing Inspection Situations
Apr 11 In this 90-minute accredited course, you will hear about real life examples of inspection issues on different topics such as Opening Day, Documentation, Tours, SME situations, Safety
Our Participants Testimonial
The presentation by Carolyn Troiana today was fantastic, both I and the QA Manager (Aaron Neighbour) loved it and had extensive conversation afterward about it. ( FDA Compliance and Mobile Applications Webinar )
Robert Friedland ( IT Manager) NUTEK BRAVO, LLC.
Thank you for providing the information in such detail. It was helpful to gain the perspective of somebody that has implemented these regulations in a working lab. Virtual Seminar on ( Training on Life cycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines )
Tracey Kessler ( Director of R&D) CEL-SCI Corporation
I felt the seminar was very helpful and provided good insight for DataIntegrity and what the FDA is looking for per the regulations. ( Current Regulatory Thinking on Data Integrity 2 Days Virtual Seminar )
Margaret A. Clifton ( Manager, Quality Systems) CSL Plasma
The presenters subject matter knowledge is extensive which enables information to be shared in detail. (Training Attended on Risk Based Verification and Validation Planning to Meed US FDA and ISO 13485 Requirements )
Stuart Chisholm (Sr. Principal Device Engineer) Teva Pharmaceuticals
About World Compliance Seminars (WCS)
World Compliance Seminars (WCS) is one stop solution for all your pharmaceutical, biotechnology and medical device certification program needs. The pharmaceutical and medical device training requirements are set forth by the FDA (Food and Drug Administration) and other major regulatory bodies like NIH, EMA, as well as numerous European based national regulatory bodies.
These requirements are important to the training of pharmaceutical reps who are responsible for the education, professional development, and on-the-job training. The training is broken down into different sections to cover a wide variety of topics, including pharmaceutical formulation, pharmaceutical transfer processes , GLP, GMP, Clinical Compliance, Process Validation, Global Regulatory Affairs, Document Management,GMP (Good manufacturing practice) QSR and CMC and many more.
The pharmaceutical and medical device requirements that the FDA has set forth are designed to protect the public's health and safety. Pharmaceutical reps must adhere to all of the regulations and education courses provided by the FDA in order to be considered one of the best in their field. They also must complete ongoing educational opportunities and maintenance programs in order to maintain relevance and career enhancement.
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