A Contract Research Organization (CRO & CDMO) for the pharmaceutical and generic drug industries - helping partners in India and around the world take products from idea to dossier with scientific expertise, quality and complete confidentiality.
Products out-licensed for EU & US markets
Global Partnerships
Formulation Development
Analytical Research
Regulatory Strategy
IP Strategy
Tech Transfer
Clinical Supplies
505(b)(2)
Generics
Formulation Development
Analytical Research
Regulatory Strategy
Formulation Development
Analytical Research
Regulatory Strategy
IP Strategy
Tech Transfer
Clinical Supplies
505(b)(2)
Generics
Formulation Development
Analytical Research
Regulatory Strategy
FTF Pharma Pvt. Ltd. was incorporated in June 2012 and serves pharmaceutical and generic drug companies across major global markets. Our purpose is to improve the quality of human lives by delivering novel, affordable pharmaceutical products based on innovation and technology.
Finished-dosage formulation development for generic and branded companies, including incremental innovation and 505(b)(2) products.
Why FTF Pharma
We combine deep formulation and patent expertise with pharmacokinetic understanding and innovative thinking in product development - backed by a dedicated team and full confidentiality.
Formulation and analytical scientists supported by a dedicated QA-IPR group.
Formulation scientists with strong patent, pharmacokinetic and regulatory understanding.
Quality built into every stage of development, documentation and data.
Formulation, analytical and stability facilities to support development through scale-up.
Engagement models tailored to each partner - from a single study to full product development.
Strict protection of partner information, data and intellectual property.
Every project follows a structured, transparent process so partners know exactly what to expect - and when.
Share your product idea or project requirement with our Business Development team.
Our scientists assess scientific, regulatory, IP and commercial feasibility.
You receive a clear proposal covering scope, timelines, deliverables and cost.
Development is carried out with defined milestones and regular progress updates.
Complete data, reports and documentation - ready for tech transfer or filing.
Our development work is designed to meet the expectations of regulators in the US, Europe and other major markets - with robust documentation, data integrity and audit readiness at its core.
Defined quality policy and procedures across development.
Development aligned to US, EU and global requirements.
From product identification and formulation development through analytical, regulatory and IP strategy to clinical supplies and technology transfer - one experienced team, one point of contact.
OSD, injectables, ophthalmic, nasal, dermal, patches & high potency
Method development, validation and stability studies
Global regulatory strategy, dossiers and query responses
Non-infringing formulation and patent strategy
Products out-licensed for EU & US markets
Differentiated generics filed in the EU through DCP
Generic products in development
Patents filed through national / PCT routes
Talk to our Business Development team about formulation development, regulatory and IP strategy, clinical supplies or technology transfer.