Dr. Syed Abid Hassan

Head of Compliance, Regulatory & Scientific Affairs at Dallah Pharma
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Jeddah, Makkah, Saudi Arabia, SA

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

5.0

/5.0
/ Based on 2 ratings
  • (2)
  • (0)
  • (0)
  • (0)
  • (0)

Filter reviews by:

Maqsood Mahmoodi

During the tenure at Jamjoom Pharma when i joind R&D Formulations as Asst. Manager, i had come across Dr. Syed Abid Hassan, who was working as Regulatory Affairs Manager, managing a team of more than 20 professionals. He was known to be the building block of Regulatory of Jamjoom pharma, which he nurtured from zerolevel. I found him honest, professional & practical. He is a very humble personality, always willing to extend helping hands to colleagues. What makes him unique is, his learning appetite & persistence in mastering it, in any field he chooses to work on. I wish him very best of luck.

Amer Alanazi, Ph.D

Abid is an exceptional trainer and professional gentleman. I have been known him for quit long time and I really admire his passion about knowledge spread and sharing among others. His vast knowledge and cumulatixlve experiences are some thing any one would appreciate amd acknowledge. I have worked with him on some projects and noticed his commitment, desire, and detailing in each aspect of that project. He cares alot for his peers and always hope the best for others. He is really fantastic guy who you can mingle and get along with easily. I would indeed recommend him for any senior position at any relevant organizations.

You need to have a working account to view this content.
You need to have a working account to view this content.

Credentials

  • ISO13485 (Quality Management System Lead Auditor Training Course) UK
    British Standards Institute (BSI) - UK
    Aug, 2016
    - Nov, 2024
  • Intensive course of Quality Assurance
    CfPA - The Center for Professional Advancement - Europe
    May, 2011
    - Nov, 2024
  • ISO 13485 (Quality Management System) specialization in Medical Device, UK
    IRCA Global
    Sep, 2016
    - Nov, 2024
  • Certified Training Professional
    Dubai Knowledge Park
  • Diploma in Computer Application
    Indian Institute of Computer Studies
  • Six Sigma Black Belt
    VMEdu Inc.
  • Six Sigma Yellow Belt
    VMEdu Inc.
  • TOT (Trainer of/for Electronic Training)
    Arabian Technology Training Center (KSA)
  • TOT (Trainer of/for Training)
    American East Coast University

Experience

    • Saudi Arabia
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Head of Compliance, Regulatory & Scientific Affairs
      • May 2021 - Present

    • Saudi Arabia
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Regulatory Compliance Head, Team Leader of Variation Management Committee, Trainer
      • Apr 2019 - May 2021

      -Final Review of dossier (NCE/Generic/Herbal/Neutraceuticals/Cosmetics) as per regulatory requirements before submission to various markets (GCC/SFDA/African Market/ASEAN/South Africa/CIS etc.).-Assessment of dossier for product submission and GAP analysis.-Responding to the deficiencies/queries-Lead Variation Management Committee for handling (Assessment and filing) for different countries-Assessment of Documents as per Guideline (Country specific/ICH).-Monitor and assess the regulatory environment.-Determine requirements and options for regulatory submissions, approvals and complianceactivities.-Develop optimal strategy for Agency interactions during product development and life cyclemanagement.- Assess quality systems (e.g., ICH, GMP/QSR, ISO, etc.)- Ensure specifications for testing of API/drug substance/drug product and documentation of rawmaterials (novel excipients, animal derived materials, etc.) comply with regulatory requirements.-Training the staffs as per the need Show less

    • Regulatory Compliance Head, Team Leader of Variation Management Committee
      • Mar 2017 - Apr 2019

    • Regulatory Compliance Head
      • Feb 2014 - Feb 2017

      Lead Review of the dossiers before submission to the Regulatory Authorities/Agencies

    • Saudi Arabia
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Manager Global Regulatory Affairs
      • Jan 2007 - Dec 2013

      -Review of template, dossier and SOP of dossier preparation for various markets.- Review of dossiers (NCE/Generic/Herbal/Neutraceuticals/Cosmetics) as per regulatory requirements (GCC/SFDA/African Market/ASEAN/South Africa/CIS etc). - Assessment of dossier for product submission and GAP analysis.- Variation handling (Assessment and filing) for different countries - Handling/Trouble shooting-eCTD (Lorenz-Docubridge)- Classification and Preparation of application for Medical Devices.- Technical File/Device Master file ----Medical Device- Assessment of Documents as per Guideline (Country specific/ICH).- Product Classification (Drugs/Herbal/Nutraceuticals/Medical Devices/Cosmetics).- Monitor and assess the regulatory environment.- Determine requirements and options for regulatory submissions, approvals and compliance activities (registration, listings, etc.).- Develop optimal strategy for Agency interactions during product development and life cycle management.- Assess quality systems (e.g., ICH, GMP/QSR, ISO, etc.)- Ensure specifications for testing of API/drug substance/drug product and documentation of raw materials (novel excipients, animal derived materials, etc.) comply with regulatory requirements. Show less

    • Assistant Manager KSA & International Markets
      • Jan 2004 - Dec 2006

    • Executive Regulatory Affairs
      • Nov 2001 - Dec 2003

      -Preparation of the Product Dossier-Review of Dossiers -Responding queries or deficiencies -Artwork preparation and review-Updation of submission and status record-Liaising with cross functional teams for catering information for the dossiers

Education

  • SSSUTM
    Doctor of Philosophy - PhD, Chemistry
  • VM Research Foundation - University
    Master of Science (M.Sc.), Chemistry
  • EILM University
    Master of Business Administration (M.B.A.), International Business
  • R.L.S. COLLEGE OF EDUCATION
    Diploma, Pharmacy

Community

You need to have a working account to view this content. Click here to join now