Life Sciences Compliance Whiz - Gold Season Ticket
1 ticket - 10 live webinars - 60 days’ access

Tap into the insights from the most experienced thought leaders in GRC to build upon your knowledge and grow as a professional. Gather valuable, real-time information and feedback to make an immediate difference to your organization.

We have built a training curriculum to help you with that – the Life Sciences Compliance Whiz – Gold Season Ticket. Learn at your own convenience with access to 10 live webinar courses for 60 days!

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About this Season Pass

Life Sciences Compliance Whiz - Gold Season Ticket gives you access to 10 instructor-led live webinars over 60 days. Now, become specialized in life sciences by learning on your own terms, whenever you want, wherever you want. Get professional training in varied industries viz. pharmaceuticals, medical devices and biologics at your convenience.

This Life Sciences season pass provides live online training on FDA regulations, guidelines and best practices. Enhance your knowledge on good manufacturing practices for pharmaceutical, auditing skills, FDA inspection, quality assurance, ISO 13485, ISO 14971 standards, EU MDD, quality system regulations, medical device reporting, computer system validation, device history records, packaging and labeling regulations, BLA, microbiological risk, contamination control, stability studies, development and approval, immunogenicity testing and much more. This pack of courses will help QA managers, laboratory personnel, analysts, consultants, bioanalytical scientists, technologists navigate through complex regulatory landscape.

Additionally, participants will become familiar with implications and application of the many guidances that apply to the marketing of life science products.

Why get this pass:

  • Most relevant Life Sciences topics covered
  • Pay once and attend any 10 instructor-led batches in 60 days
  • Learn from the comfort of your home\office
  • Maximize your training with our highly experienced trainers
  • Build expertise in industry-specific compliance requirements
  • Demonstrate your commitment to staying current in the field of Life Sciences
  • Get certified on course completion

Note: This offer cannot be clubbed with any other offer.

Life Sciences Regulations & Compliance Training

Designing Medical Device Alarms to Mitigate New FDA Concerns 23-May-2017

How has the rapid growth of low-cost wearable health monitors, such as those worn on the wrist or clothing, changed data collection in clinical trials 23-May-2017

Best Practices for FDA and ISO 13485 Corrective Actions 25-May-2017

What exactly is required for 21 CFR Part 11 compliance 25-May-2017

Understanding and Implementing a Technology Transfer Process 25-May-2017

Best Practices for Investigating Deviations 26-May-2017

CSV 21 CFR part 11 30-May-2017

Best Practices to Assure Prompt Review, Disposition and Control of Nonconforming Product 30-May-2017

3-hr Virtual Seminar: Validation and Part 11 Compliance of Computer Systems 30-May-2017

6-hr Virtual Seminar: Process Validation for Drugs and Biologics 31-May-2017

3-hr Virtual Seminar: Japan Regulatory Compliance Requirements for Life Science Products 02-Jun-2017

Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467> 05-Jun-2017

6-hr Virtual Seminar-FDA Software Regulation, Cybersecurity Requirements and Interoperability 06-Jun-2017

Establish and Maintain an Effective Supplier Qualification Program 06-Jun-2017

FDA Regulations for Cosmetics & New Legislation 06-Jun-2017

Common Problems and Mistakes in Method Validation in Drug Development Process 07-Jun-2017

Federalwide Assurances: What are they; why and when do I need them? 08-Jun-2017

The 510(k) Submission: Requirements, Contents, and Options 09-Jun-2017

Critical Elements of Quality Risk Management Relating to FDA Compliance 14-Jun-2017

Risk Based Medical Device Design Control 15-Jun-2017

Efficient and Effective FDA and ISO Management Reviews 22-Jun-2017

Understanding and Implementing a Quality by Design Program 23-Jun-2017

3 Hour Virtual Seminar : Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process 27-Jun-2017

The Use and Misuse of FMEA in Medical Device Risk Management 28-Jun-2017

3-Hour Virtual Seminar: Validation Challenges for Bioassays 28-Jun-2017

Implementing a Change Control Quality System Successfully 29-Jun-2017

The Sunshine Act: Reporting for Clinical Trials 07-Jul-2017

CE Marking: Obtaining and Maintaining EU Compliance Under the Medical Device Directive 11-Jul-2017

Qualification of contract manufacturer organizations based on practical experience 20-Jul-2017

FDA Regulations for Marketing & Labeling OTC Drugs in the U.S 25-Jul-2017

Best Practices to Assure Prompt Review, Disposition and Control of Nonconforming Product 30-May-2017