![DRAP Guidance on Clinical Trials Applications: CGP Compliance Audits and Reports](https://www.regdesk.co/wp-content/uploads/2022/07/Blog-post.webp)
Jul 1, 2022
Asia
The new article describes in detail the regulatory matters related to audits or inspections for GCP compliance, as well as the reports and final application review. Table of Contents The Drug Regulatory Authority of Pakistan...
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![DRAP Guidance on Clinical Trials: Import, Timelines, and Ethical Approval](https://www.regdesk.co/wp-content/uploads/2022/06/Drap-prohibits-doctors-prescribing-brands-medicines.jpeg)
Jun 20, 2022
Asia
The new article provides additional details regarding the regulatory requirements for the importation of investigational products, as well as other aspects. Table of Contents The Drug Regulatory Authority of Pakistan (DRAP),...
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![DRAP Guidance on Clinical Trials: Application in Detail](https://www.regdesk.co/wp-content/uploads/2022/06/istockphoto-678853788-612x612-1.jpeg)
Jun 16, 2022
Asia
The new article describes in detail the procedure to be followed when applying for permission to conduct clinical trials in Pakistan. Table of Contents The Drug Regulatory Authority of Pakistan (DRAP), a country’s regulatory...
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![DRAP Guidance on Clinical Trials Applications: Overview](https://www.regdesk.co/wp-content/uploads/2022/06/istockphoto-1186916378-612x612-1.jpeg)
Jun 6, 2022
Asia
The article provides an overview of Pakistan’s regulatory framework for clinical trials and applications to be submitted by interested parties. Table of Contents The Drug Regulatory Authority of Pakistan (DRAP), a country’s...
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![DRAP Guidance on Imports & Exports of Therapeutic Goods: Overview](https://www.regdesk.co/wp-content/uploads/2022/04/partial-photograph-girl-doctor-nurse-stethoscope-uniform-against-background-national-flag-state-pakistan-concept-158166201.jpeg)
Apr 13, 2022
Asia
The article provides a brief overview of Pakistan’s regulatory requirements in the sphere of importation and exportation of medical devices and highlights the key points to be considered by medical device manufacturers and other parties involved in placing medical...
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