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Results for tag: "Regulatory Affairs"

UAE Pharmaceutical CRO Market, By Region, Competition, Forecast and Opportunities, 2020-2030F - Product Thumbnail Image

UAE Pharmaceutical CRO Market, By Region, Competition, Forecast and Opportunities, 2020-2030F

  • Report
  • January 2025
  • 82 Pages
  • United Arab Emirates United Arab Emirates
From
UAE Contract Manufacturing Organizations Market, By Region, Competition, Forecast and Opportunities, 2018-2028F - Product Thumbnail Image

UAE Contract Manufacturing Organizations Market, By Region, Competition, Forecast and Opportunities, 2018-2028F

  • Report
  • November 2023
  • 77 Pages
  • United Arab Emirates United Arab Emirates
From
Saudi Arabia Biotechnology And Pharmaceutical Services Outsourcing Market, By Region, Competition, Forecast & Opportunities, 2020-2030F - Product Thumbnail Image

Saudi Arabia Biotechnology And Pharmaceutical Services Outsourcing Market, By Region, Competition, Forecast & Opportunities, 2020-2030F

  • Report
  • March 2025
  • 85 Pages
  • Saudi Arabia
From
UAE Biotechnology and Pharmaceutical Services Outsourcing Market, By Region, Competition, Forecast and Opportunities, 2020-2030F - Product Thumbnail Image

UAE Biotechnology and Pharmaceutical Services Outsourcing Market, By Region, Competition, Forecast and Opportunities, 2020-2030F

  • Report
  • January 2025
  • 82 Pages
  • United Arab Emirates United Arab Emirates
From
Saudi Arabia Pharmaceutical CRO Market, By Region, Competition, Forecast and Opportunities, 2020-2030F - Product Thumbnail Image

Saudi Arabia Pharmaceutical CRO Market, By Region, Competition, Forecast and Opportunities, 2020-2030F

  • Report
  • January 2025
  • 80 Pages
  • Saudi Arabia
From
Neurology Contract Research Organization Market - Global Industry Analysis, Size, Share, Growth, Trends, and Forecast 2031 - By Product, Technology, Grade, Application, End-user, Region: (North America, Europe, Asia Pacific, Latin America and Middle East and Africa) - Product Thumbnail Image

Neurology Contract Research Organization Market - Global Industry Analysis, Size, Share, Growth, Trends, and Forecast 2031 - By Product, Technology, Grade, Application, End-user, Region: (North America, Europe, Asia Pacific, Latin America and Middle East and Africa)

  • Report
  • January 2024
  • 244 Pages
  • Global
3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH - Product Thumbnail Image

3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH

  • Training
  • 3 Hours
  • Global
GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers (Recorded) - Product Thumbnail Image

GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers (Recorded)

  • Training
  • March 2024
  • 6 Hours
  • Global
From
The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded) - Product Thumbnail Image

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers (Recorded)

  • Training
  • February 2024
  • 2 Days
  • Global
From
The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded) - Product Thumbnail Image

The US FDA QMSR Transition - 21 CFR 820 and ISO 13485 (Recorded)

  • Training
  • February 2024
  • 90 Minutes
  • United States
From
Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded) - Product Thumbnail Image

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations (Recorded)

  • Training
  • August 2023
  • 2 Days
  • Global
From
USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms - Product Thumbnail Image

USP <61>/<62> Microbiological Enumeration and Examination of Non-Sterile Products - Understanding the Current Standards for the Revised USP and Harmonized EP Microorganisms

  • Training
  • 90 Minutes
  • Global
Surviving an FDA Sponsor Inspection - Training for Success - Product Thumbnail Image

Surviving an FDA Sponsor Inspection - Training for Success

  • Training
  • 105 Minutes
  • Global
The 510(k) Mod Program, Breakthrough Technologies, and STeP (Recorded) - Product Thumbnail Image

The 510(k) Mod Program, Breakthrough Technologies, and STeP (Recorded)

  • Training
  • August 2024
  • 90 Minutes
  • Global
Understanding and Preparing for FDA Pharmaceutical Inspections (Recorded) - Product Thumbnail Image

Understanding and Preparing for FDA Pharmaceutical Inspections (Recorded)

  • Training
  • June 2024
  • 90 Minutes
  • Global
Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance (Recorded) - Product Thumbnail Image

Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance (Recorded)

  • Training
  • June 2024
  • 90 Minutes
  • Global
Assess Impact For Supplier Change Notices (Recorded) - Product Thumbnail Image

Assess Impact For Supplier Change Notices (Recorded)

  • Training
  • June 2024
  • 60 Minutes
  • Global
eCTD Submissions - Fundamentals and Process (Recorded) - Product Thumbnail Image

eCTD Submissions - Fundamentals and Process (Recorded)

  • Training
  • February 2024
  • 60 Minutes
  • Global
From
Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance (Recorded) - Product Thumbnail Image

Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance (Recorded)

  • Training
  • December 2023
  • 2 Days
  • Global
From
Audit Like the FDA - Effective Internal Audit Program (Recorded) - Product Thumbnail Image

Audit Like the FDA - Effective Internal Audit Program (Recorded)

  • Training
  • July 2023
  • 2 Days
  • Global
From
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Regulatory Affairs in the biotechnology industry is the process of obtaining and maintaining approval from regulatory authorities for the development, manufacture, and marketing of biotechnology products. This includes the submission of applications, such as Investigational New Drug (IND) applications, New Drug Applications (NDAs), and Biologics License Applications (BLAs). Regulatory Affairs professionals are responsible for ensuring that biotechnology products comply with applicable laws and regulations. Regulatory Affairs professionals must have a thorough understanding of the regulatory environment and the ability to interpret and apply regulations to the development and marketing of biotechnology products. They must also be able to effectively communicate with regulatory authorities and other stakeholders. Companies in the Regulatory Affairs market in the biotechnology industry include Parexel, Quintiles, Covance, PRA Health Sciences, and Charles River Laboratories. Show Less Read more