Top Pharmaceutical and Medical Device Trainings in 2023
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
June 05-06 In this two day workshop conference you will learn the requirements and expectations of major health care regulators that are applicable to "virtual" companies
Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations Training
June 06 The objective of this live training webinar is to develop an understanding of how a compliant laboratory handles the investigation of OOS test
The Project Management Plan
June 06 This webinar will introduce the concept of planning and how it is conducted. During the webinar
Mobile Device Apps and the FDA – Classification, Regulatory Requirements and Cybersecurity
June 07 This has resulted in the FDA focusing on the subset of software functions dealing with medical issues which the Agency intends to apply its authority
Project Management for Non-Project Managers – PM in the Life Sciences – Pharmaceutical/ Biotechnology and Medical Devices
June 12-14 This virtual seminar will address those project management critical tasks within each project phase that must be performed flawlessly for effective
Analytical Method Validation, Verification and Transfer
Jun 07-08 In this course, general guideline for the determination of the analytical characteristics for different types of validation procedures
FDA's regulation of Promotion and Advertising
June 08 The seminar will cover topics that equip you with the knowledge and skills required to avoid the FDA’s enforcement hammer
2 Day Virtual Seminar on FDA Inspection Essentials in 2023
June 13-14 This seminar, you will learn how to properly alert key members that an investigator has arrived, the proper protocol
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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