Advancing Health,, Ensuring Quality, Delivering Trust
What Sets Us Apart What It Means for You
End-to-End Pharma Expertise
From R&D formulation to regulatory filing to manufacturing and delivery — all under one roof.
Regulatory & Compliance Focus
Quality at Every Step
Scalable & Flexible Operations
Innovation Driven
We don’t just replicate — we improve, adapt, and seek better ways to solve pharmaceutical challenges.
Achieving Your Vision
Planning for retirement is essential to your long-term financial well-being. At Finovate, our experienced team collaborates with you to identify your retirement goals and crafts a tailored, comprehensive strategy to help you achieve them with confidence.
What We Provide
Drug Formulation & Development
Manufacturing & GMP Compliance
Quality Assurance & Control
Regulatory Affairs & Compliance
We help you navigate the complex regulatory landscape — approvals, filings, licensing, documentation for domestic and international markets. Staying up to date with national regulatory agencies and global standards ensures faster time-to-market and risk mitigation.
Packaging, Labelling & Serialization
Supply Chain & Distribution
Ensuring that your product moves from plant to patient efficiently. Cold chain where required, warehousing, logistical compliance, traceability, shelf-life optimisation, inventory management, and demand forecasting.
Research & Innovations
Continuous innovation is key — be it novel drug delivery systems, improved bioavailability, generic drug development, or parsing opportunities in biologics or biosimilars. We engage in R&D collaborations, lab capability enhancement, patent analysis, and lifecycle management.
See What Our Clients Are Saying
Our Process
Discovery & Requirement Assessment
We begin with understanding therapeutic goals, target patient population, regulatory territory, competition, route of administration, dosage form, and formulation constraints.
Pilot Production & Process Validation
Scale up to pilot batches, validate manufacturing processes, ensure reproducibility, establish specifications.
Formulation Design & Pre-Clinical Evaluation
Laboratory formulation, stability studies, excipient compatibility, assay method development, preclinical safety profiling as needed.
Commercial Manufacturing & Quality Monitoring
GMP-compliant production, batch consistency, testing, ongoing stability & shelf-life studies, surveillance of adverse reactions or product complaints.
Regulatory Submission & Approval
Compilation of dossiers, clinical / bioequivalence data (if applicable), packaging & labelling packs, obtaining required licences & clearances, both local (national regulatory bodies) and international where relevant.
Distribution, Post-Market Surveillance & Lifecycle Management
Secure supply chain, cold chain management if relevant, monitoring of market performance and feedback. With changing market or therapeutic needs, updating formulations, packaging or introducing variants.
