President and Group CEO
Sr Consultant GxP, Principal Auditor/Inspector and Lead Trainer
With a wealth of over 26 years of global experience, Dr. Choudhary has been based in the UK for the past 16 years. He boasts a solid track record, having conducted more than 500 audits and inspections, and successfully overseen over 48 inspections in the last decade from esteemed agencies such as the US FDA, EMA, MHRA, HPRA, AEMPS, TGA, ANVISA, WHO, SFDA, CFDA, and others. His expertise spans across various GCP topics, Inspection Readiness, Risk-based Vendor and Audit Management, IT Systems Validation, Data integrity, and more.
He has played a pivotal role in conducting gap assessments, revamping or establishing QMS afresh, and providing team training on various GxP topics to assist organizations in embracing a Quality by Design approach.
Dr Choudhary is author of two books on Pharmaceutical sciences and holds a PhD and MD degree as well.
Head of Business and Regulatory Intelligence
Founder, FemX (UK and Pakistan's first Women-led App)
Mrs Almas has a Masters in Microbiology and brings with her over 22 years of experience within Regulatory Intelligence. She spearheads business innovation at LabQ and is also founder of UK and Pakistan's first women-led application for women health and hygiene called FemX.
A highly accomplished Quality Assurance and Validation professional with over 25 years of experience across the pharmaceutical, biotechnology, medical device, and ATMP (Advanced Therapy Medicinal Products) sectors. Demonstrated expertise in developing, implementing, and managing robust Quality Management Systems (QMS) that ensure full cGMP and GxP compliance in alignment with international regulatory requirements.
Proven success in leading US FDA/MHRA remediation initiatives and ensuring Pre-Approval Inspection (PAI) readiness, as well as providing comprehensive support during regulatory inspections by agencies such as the MHRA, FDA, and others. Skilled in conducting gap assessments and applying Operational Excellence tools, including FMEA, Process Mapping, Fishbone Analysis, 5 Whys, 1H 5W, and Root Cause Analysis (RCA).
Dr Syed holds a PhD in Pharmacy and a subject matter expert on equipment commissioning and qualification as well as cleaning validation and CMC processes.
Sr Consultant CMC, GMP and GLP Quality
Experienced Senior Consultant specializing in CMC, GMP, and GLP Quality Assurance. With over 26 years in the biopharmaceutical industry in the UK, Tallat's expertise includes supplier evaluation, auditing, QMS management, GXP compliance, training, batch release, and QC. He has worked with top global pharmaceutical companies like AstraZeneca and GSK as well as small biotech startups. Skilled in evaluating QA compliance with international GXP regulations, and excels in implementing best quality practices for investigational medicinal products and marketed drugs. Tallat has a proven track record of delivering significant outcomes and have conducted numerous GXP audits and regulatory inspections worldwide, including FDA and MHRA evaluations.
Tallat holds Masters degree in quality and international business administration from UK and Europe. Lead auditor qualifications in both PQS and ISO QMS.
We allocate dedicated Project Managers for each project
(regardless of its size) and deliver Quality Right First Time
