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Specialized Expertise: Solid Oral Dosage (Tablets & Capsules) Formulation & Dissolution
The scope involved pharmaceutical formulation development for immediate and sustained-release solid oral dosage forms. The engagement covered binder-excipient compatibility screening, fluid-bed granulation parameters, tablet hardness-friability optimization, and f2 similarity factor dissolution testing against innovator drugs. The deliverables provided complete Batch Manufacturing Records (BMR) and technology transfer dossiers.
To protect non-disclosure terms and proprietary assets, identifying client identities, commercial budgets, and location specifics are withheld from public display.
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