Development and Manufacturing of FDFs

Formulation Development is a process in which one or more therapeutically active ingredients are combined usually with more than one excipient to prepare area pharmacologically active composition. The process aims to impart stable shelf life while adhering to all regulatory requirements and making the formulation of patient complaint.

API Pharma Tech LLC has a well-equipped, dedicated Formulation and Development (F&D) laboratory. These include oral dosage forms (Tablet, capsules, powders and Liquids), Parenteral Dosages (Sterile liquid, suspension, Freeze dried powder), Topical Dosages (Creams and Ointments, Lotions), Ophthalmic Dosages (Sterile Solutions and suspensions). A separate Analytical Development Laboratory, equipped with latest instruments, is also present to support the formulation development activities.

Our team of dedicated scientists constantly works for the betterment of society focusing on the following activities:

  • Designing dosage forms by using the most innovative techniques to meet the safety, quality and therapeutic efficacy.
  • Developing analytical methods of evaluation and subsequent validation and to lay down finished product specifications by all regulatory compliances. Continual development of existing products to meet customer satisfaction.
  • Interacting with technical teams through training programs to facilitate regular exchange of ideas regarding any new products and to create awareness about the latest technologies and research