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International Webinar on Materials Science and Engineering 2022 London United Kingdom

International Vein Conference 2022 Miami Beach United States

International Vein Congress 2022 Miami Beach United States

Imparting Practice Consensus and Cutting-edge Information

Internal Auditing to MDSAP: Concepts and Practices in Aligning the Internal Audit Program 2022

Reviewing Drug Product Batch Records 2022

Batch record review is an important step in the release of a medicinal product. This webinar sets out the regulatory requirements for batch records and sets out a systematic approach for review. Trending of batch data is also discussed.

Breaking the Mold: Best Practices for Mycotoxins Prevention and Control in Food 2022

Case Management Outcomes: How to Know if you are Working in a Best Practice Framework 2022

Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do 2022

FDA's Ambitious Regulation of Social Media 2022

Troubleshooting Dissolution Methods for Solid Oral Dosage Forms 2022

Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations 2022

How to Prepare a Standard Operating Procedure (SOP)? 2022

This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time.

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices 2022

21st World Congress on Nursing 2022

International Conference on Cell & Stem Cell Research 2022 Paris France

International Conference and Expo on Applied Microbiology 2022 rome Italy

53rd World Congress & Expo on Advanced Nursing and Nursing Practice 2022 osaka Japan

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24th International Conference on Cardiology Insights. 2022 Tokyo Japan

3rd Edition of International Precision Medicine Conference 2022 London United Kingdom

International Conference and Expo on Clinical Microbiology 2022 Rome Italy

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation 2022

SOP Writing, Training and Compliance in the Pharmaceutical Industry 2022

Process Validation Guidance Requirements 2022

21 CFR Part 11 Compliance for SaaS/Cloud Applications 2022

This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.