Karim Panjwani

Karim Panjwani, a pharmacist, quality assurance professional, and technical writer, brings over 17 years of experience in the pharmaceutical industry. He has collaborated with leading multinational companies to establish quality systems that adhere to various regulatory bodies, including the U.S. FDA, MHRA, EU GMP, Health Canada, TGA, ANVISA, and WHO Geneva.

His area of expertise encompasses oral solid dosage, sterile, and nasal formulations. He possesses a profound understanding of the manufacturing and utility equipment used in pharmaceutical formulation production. Karim is adept at drafting and editing technical documents such as procedures, processes, investigations, risk assessments, and regulatory communications. He has a comprehensive understanding and practical knowledge of global regulations concerning the manufacture, storage, and distribution of pharmaceutical medicines.

Karim is passionate about disseminating his knowledge and insights through his papers and blogs. These cover a range of topics, including good documentation practice, regulatory expectations, quality culture, and cleaning validation.