Regulatory due diligence in the pharmaceutical industry involves the thorough examination of a company’s compliance with relevant regulatory standards and guidelines. This process ensures that the company adheres to laws governing drug development, manufacturing, marketing, and distribution. Key aspects include reviewing the company’s regulatory submissions, approval status, clinical trial data, and adherence to Good Manufacturing Practices (GMP). It also covers the assessment of intellectual property, licensing agreements, and potential risks from non-compliance. Regulatory due diligence is crucial during mergers, acquisitions, and partnerships to minimize risks and ensure smooth market......See More