This includes the development of product formulation, manufacturing process, and analytical procedures for the following dosage forms:

• Simple oral dosage forms (Immediate release (IR) tablets, Orodispersible and chewable tablets, Oral solutions, and suspensions)
• Complex solid dosage forms (Extended-Release (ER) products, Multilayer tablets, Multiparticulate system, Soft gelatin capsules) 
• Transdermal (ointments and gels)
• Simple sterile liquids (Vials, ampoules, Pre-filled syringes)
• Complex injectables (Lyophilized, Extended release injectables/Injectable suspensions (excluding liposomal), Non-aqueous formulations, Emulsions)

• Validation of manufacturing and analytical procedures/methods.
• Stability: Execute official stability batches and stability testing program.
• Documentation: Generate official documents needed for the registration of the drug product.
• Transfers: Handle project transfers to Tech transfer centers and Contract Manufacturing Organizations (CMOs).