This document provides information about an upcoming training session on Good Manufacturing Practices. The session will be held on October 16th in Karachi and will run from 9:00 am to 3:00 pm. It is aimed at pharmaceutical professionals with backgrounds in pharmacy, chemistry, microbiology and related fields. Experts from the US pharmaceutical industry will discuss advancements in manufacturing technology and emerging regulatory changes. The session will include tutorials, discussions, and Q&A to help participants better understand GMP requirements and ensure quality assurance. Participants will pay Rs. 10,000 or Rs. 5,000 depending on whether they are attending as part of their job. More details and contact information are provided.

2. 119th
CCK & 9th
CQS Session
What is New & Coming in
Good Manufacturing Practices
Date & Venue: InshaAllah on 16th
October 2022, Sunday at Hotel Regent Plaza or
Marriott, Karachi
Timings: 09.00 - 10.00 am – Harmonizing Exercise on subject through video,
discussion on phenomena.
10.00 am to 03.00 pm - Tutorial, Question & Answer and Take Home
Messages (Tea and lunch will be served).
Eligibility: Practicing Pharmaceutical Professionals having background education of
Pharmaceutical Sciences (BPharm or PharmD), Chemistry, Microbiology,
Biochemistry, Molecular Biology, Applied Chemistry and Engineering.
Expert Sharing: US based richly experienced leading professionals (with Pharmacy,
Chemistry & Engineering educational background) currently working for
different pharmaceutical industries will be talking on the subject. Adviser
CQS, Obaid Ali will be coordinating the session.
Key Learning Objectives: Advancement in pharmaceutical manufacturing technology, complexities
of manufacturing processes and products, reshaping of regulatory frames
and emerging paradigm shifts will be focused throughout the day. Program
is designed to try answering the questions in simple, clear and with sound
expression supported by real time examples on the topic and related
contemporary subjects.
Petition of the Program: A blog entitled “Honest Transformation to Maintain Momentum in
Assurance of Drug Quality” is the source thought. A system cannot be
mature without maturing the personnel operating the quality system at any
shell. Education and training are important but not sufficient to develop
personnel unless one learns to connect data to information and sketch
design from information to knowledge through feelings and experiential
learning. Complete blog may be read on www.orcqs.com.
Methodology: Tutorial will be accompanied by interactive discussion to initiate thinking
process and keep aligned with the objectives of the subject. Real time
examples and case studies pertaining to the topic will be used to describe
the scenarios and regulatory expectations.
Group Size: It will be small to maintain direct supervision during the training and
exercises.
Fellowship Available: Write detail message of interest and justification for applying fellowship.
It will be kept confidential and respected.

3. Fee: Rs. 10,000/= per participant for companies
Rs. 5000/= per participant, if he is paying from his or her salary
Obaid & Roohi Centre for Quality Sciences
Allied Bank, Allama Iqbal Road Branch (Code: 0663)
Account No. 0010030041080020
Contacts: WhatsApp 0321-5150062 or send email at cqsciences@gmail.com
For Questions: Please write at cqsciences@gmail.com
Faculty: Obaid Ali & Mrs. Roohi B. Obaid
Alumni of University of Karachi with postgraduate degrees in
pharmaceutical sciences, Alumni of International Forum of Regulators
CDER, US-FDA & HPFB, Health Canada. Richly experienced with hands
on practice in applied regulatory sciences. Author of high impact policies,
guidance. Architect of critical regulatory reforms and investigator of
several national cases & GMP tragedies. Training Consultant for UN –
WHO & international agencies. Teacher, writer, member of different
academic boards & professional organizations. Presented hundreds of
lectures within and outside the country. Worked on different regulatory
agency desks as functional head including pre and post registration of
drugs, compliance and enforcement of manufacturing facility, governing
policy, designing initiatives, developing strategies and conducting
trainings within the country, regulatory agency and outside Pakistan.
Extensive experienced based knowledge on assessment of pre and post
market affairs, compliance & enforcement. Key officers in developing
regulatory strategies, approaches, tools and standards during constitutional
driven transformation within government. Conducted academic courses &
supervised post graduate students of health sciences, biological sciences,
pharmaceutical sciences for their MS, Ph. D. research work.
Website: WWW.ORCQS.COM visit for further information.