Life Science Training Institute, FDA Regulatory Compliance Training Online

WCS is Training Institute provides best certificate courses online for the pharmaceutical, FDA, Life Science, Biotech, Medical Device, and Skin/Cosmetics Industries

Top Pharmaceutical and Medical Device Trainings in 2022

Investigation of Out-of-Specification Test Results

25 Jan Attendees will learn the FDA expectations when investigating out-of-specification and out-of-trend laboratory results.

Paul Larocque

$265

FDA Compliance and Enforcement Trends focused on Data Integrity

26 Jan This course will enable you to best anticipate and prepare for FDA scrutiny, understand your role during inspections and audits

Carolyn Troiano

$249

Purchasing Controls, Receiving Inspection, and Supplier Audit – what to do during a global pandemic

27 Jan This webinar will provide insights into how to use remote auditing techniques to minimize the risk and maximize the benefits of conducting audits

Susanne Manz

$249

Lyophilization Basics for Pharmaceuticals: History, Scientific Principles, Cycles and Formulations

Jan. 27, 2022 To learn the how and why for formulating and designing lyophilization cycles for drugs that will benefit from the freeze-drying process

Lisa Hardwick Thompson

$595

Basic GMP Training for the QC Laboratory

Jan 31- Feb 03 This course will provide participants with an understanding of how to effectively handle out-of-specification

Kelly Thomas

$1,495

Developing an Effective Strategy for Testing Raw Materials in Phase 1 Through Phase 3 Environment

02 Feb This live training will cover testing requirements during each Phase and what may be optional until the product moves to its next Phase

Barry A. Friedman

$299

Death by CAPA - Does your CAPA Program need a CAPA?

Feb 04 This seminar will cover regulatory expectations, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls

Susanne Manz

$850

Dealing with Out of Specification Test Results in FDA Regulated Industries

Feb 08 This webinar with a thorough knowledge on what is allowed and what is not allowed and areas that need to be looked at for a thorough investigation

Meena Chettiar

$199

U.S. FDA and EU Medical Device Directive Requirements for DHFs, DMRs, DHRs, and TF/DDs

Feb 09 This webinar will examine the existing and proposed requirements for the U.S. FDA’s DHF, 21 CFR 820.30 and now ISO 13485:2016 7.3

John E Lincoln

$499

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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