Biography

About the Instructor

Medhat H. Alshazly is a Formulation Lab Head and Senior Pharmaceutical R&D Expert with over 10 years of hands-on experience in pharmaceutical, nutraceutical, and veterinary product development. He has led complex projects across Egypt, Saudi Arabia, and the UAE, developing more than 50 advanced pharmaceutical formulations, including extended-release tablets, bilayer systems, enteric-coated products, parenteral injectables, ophthalmic and veterinary dosage forms, and nano/microencapsulated products.

Medhat combines deep technical expertise with project leadership, guiding products from formulation design and scale-up to regulatory approval. He is highly experienced in cGMP, ICH, FDA, EMA, ANDA, SFDA, and GCC regulatory frameworks, making his courses highly practical and industry-ready.

At PharmaCores, Medhat’s teaching focuses on bridging academic knowledge and real-world industrial challenges, helping learners master the science, strategy, and problem-solving skills required to succeed in pharmaceutical R&D and production.

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Education

• Bachelor’s Degree in Pharmaceutical Sciences
  Faculty of Pharmacy, Tanta University, Egypt

• Master’s Degree Student in Pharmaceutical Technology
  Faculty of Pharmacy, Tanta University, Egypt

• PMP – Project Management Professional
  Project Management Institute

• Courses in DOE & QbD, USP Impurities, Pharmaceutical Development
  Tanta University

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Professional Experience

• Formulation Lab Head
  Nawah Scientific (2022 – Present)

• R&D Consultant & Manager (Part-Time)
  Organix & Multiple Food Supplement Manufacturers (2020 – Present)
  Leading new product development, technical file creation, and machinery qualification

• R&D Supervisor
  Averroes Pharma (2019 – 2022)

• R&D Senior Specialist
  Pharmed Healthcare – Hetero Egypt (2017 – 2019)

• R&D Specialist
  Sigma Pharmaceutical Industries (2014 – 2017)

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Areas of Expertise

• Advanced Pharmaceutical Formulation & Development

• Extended-Release, Bilayer, Enteric-Coated Tablets

• Parenteral, Ophthalmic, Veterinary, and Nutraceutical Products

• Microencapsulation & Nanoformulation Techniques

• Regulatory File Preparation (CTD, Quality File)

• cGMP, ICH, FDA, EMA, ANDA, SFDA, GCC Compliance

• Troubleshooting & Scale-Up for Complex Formulations

• Project Management & Cross-Functional Team Leadership

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Academic & Industry Contributions

• Led the development of 50+ challenging pharmaceutical formulations

• Responsible for technical files, regulatory submissions, and machinery validation

• Supervised R&D teams and mentored junior scientists

• Active contributor to innovation in advanced dosage forms

Courses