Dr. Mohammed Wasim, Pharm.D Email & Phone Number

Dubai, United Arab Emirates

Dubai, United Arab Emirates

• Led the preparation and submission of regulatory dossiers for pharmaceuticals and medical devices with the Ministry of Health (MOH) in the UAE, ensuring compliance with local regulations and industry standards.• Managed the registration process for cosmetics and supplements with the Dubai Municipality (Montaji).• Oversaw the entire regulatory submission process, including the collection, compilation, and submission of documentation, as well as follow-up with regulatory authorities to address queries and facilitate approvals.• Successfully navigated complex regulatory environments, contributing to the effective registration and market entry of various pharmaceuticals and medical devices.

Bengaluru, Karnataka, India

• Academic Ward round experience across various departments, including General Medicine, Pediatrics, Orthopedics, General Surgery, Dermatology, and Pharmacy gaining invaluable insights into clinical practices and patient care.• Conducted meticulous medication error analysis, patient counseling, prescription auditing, and adverse drug reaction (ADR) identification, ensuring compliance with regulatory standards and patient safety protocols.• Collaborated closely with healthcare professionals to optimize patient care plans, emphasizing adherence to regulatory guidelines and best practices.• Managed drug-related queries and clinical interventions with precision and efficiency, aligning with quality standards.• Actively engaged in interdisciplinary team meetings, fostering collaboration and discussion on patient cases and treatment strategies.• Stayed abreast of the latest pharmaceutical research and advancements through literature reviews and continuous learning initiatives, enhancing regulatory knowledge and professional development.• Engaged in workshops and training sessions to further enhance skills and knowledge in pharmaceutical regulations and compliance practices.

Bengaluru, Karnataka, India

• Developed a comprehensive understanding of regulatory requirements and adherence to research protocols within the pharmaceutical industry.• Assisted in formulating and implementing Standard Operating Procedures (SOPs), ensuring compliance with regulatory standards, and fostering systematic and quality-driven research processes.• Contributed to the design and development of research protocols, demonstrating proficiency in planning and executing regulatory-compliant research studies.• Assisted in the development of a multi-center, single-arm study titled 'Extracorporeal Bioengineered Dual-Cell Liver Regeneration System'• Conducted extensive research on regulatory frameworks such as Good Clinical Practice (GCP)• Guidelines and New Drug Clinical Trials (NDCT) Guidelines, ensuring adherence to industry standards and regulations.• Performed routine audits of treatment charts in the ICU wards, identifying and rectifying any discrepancies to ensure patient safety.• Contributed to the development and maintenance of regulatory databases and documentation systems to track study progress and regulatory submissions.• Contributed to the Antimicrobial Stewardship Review, highlighting a commitment to public health and responsible use of medications.

Doctor Of Pharmacy - Pharmd, Pharmacy, Distinction

Activities and Societies: 1. RGUHS Karnataka State level Football Team / Pharmacy Football Team 2. GMPSIR Karnataka State Level.

Regulatory Affairs Gcc Certification

Drug Development Product Management Specialization, Coursera, 94.72%

Education record

Doctor Of Pharmacy, Distinction

Activities and Societies: RGUHS Karnataka State level Football Team