Creative Biolabs' scientists have a wide and varied background of pharmaceutical development experience across an extensive range of compounds. Our facilities were designed to be flexible and are capable of handling a wide variety of batch sizes. We have formulation capabilities covering formulation development for early safety studies, prototype formulations for clinical trials, preliminary process identification, and commercial formulation development including generic drugs.
At Creative Biolabs, we have the expertise to formulate and develop a variety of dosage forms, including:
Formulation Development
Phase I to III Clinical Development (NCEs)
Powder-in-bottle to Drug-in-capsules
Liquid filled capsules
Comparator Studies
Formulation Development in Various Dosage Forms
Conventional Oral Solid Dosages
Press coated tablets (Sub Coated Tablets)
Bi-layered
Granules for Reconstitution
Sterile Liquids – Injectables & Ophthalmic
Non- Sterile Liquid Oral Formulations
Semi Solid Formulations
Lyophilized Products
In-situ Salt Formations
Sterile Solutions, Nanoparticles & Liposomes
Oral Solutions & Suspensions
Generic and Innovative Products
Paediatric formulations
Oncology Molecules (Sterile and Solid Dosages)
Complete development of ANDAs / CTDs
Pilot GMP manufacturing suites to support Clinical / BE studies
Preformulation Studies
Selection of form
Salt screening
Polymorph screening
Co-crystal screening
Physico-chemical characterization
pH Solubility & Stability
Solubility in bio-relevant medium
Solubility enhancement
Solid state stability
Forced degradation study
Stability indicating method development
Determination of Log P, Log D and pKa
Excipient compatibility
All listed services and products are For Research Use Only. Do Not use in any diagnostic or therapeutic applications.