the regulatory and operational groundwork, done properly.
Savison Life advises Indian pharmaceutical manufacturers and brand owners on compliance, quality systems, manufacturing operations, product development and commercial strategy — the work that decides whether a product reaches market cleanly or stalls in review.
five areas of practice.
Engagements are scoped to the problem in front of you — a licence pathway, an audit observation, a line that is losing yield, a portfolio decision.
regulatory compliance
Licensing, CDSCO and state drug authority requirements, and documentation that holds up under inspection.
Read more →02manufacturing optimization
Yield, changeover, capacity and cost — finding where a line actually loses time and money.
Read more →03quality assurance
GMP systems, deviation and CAPA handling, and the quality practice that keeps them working.
Read more →04product development
Taking a formulation from concept to a manufacturable, stable, documented product.
Read more →05business strategy
Portfolio, pricing, sourcing and go-to-market decisions for pharmaceutical businesses.
Read more →not sure which?
Describe the problem and we will tell you whether it is something we can help with — and if it is not, we will say so.
grounded in what your site can actually execute.
Assessment before advice
Every engagement starts by establishing the current position — licences held, systems in place, how the line actually runs — rather than applying a template.
Documentation that survives scrutiny
Regulatory work is judged on paperwork. We leave you with documentation an inspector or a reviewer can follow, not a summary deck.
Prioritised by return
Gap lists are easy to produce and hard to act on. Findings come ranked by what they cost you and what closing them takes.
Capability transfer
Where it makes sense, we train your team to run the process afterwards instead of creating a standing dependency.
programmes for pharmaceutical teams.
Structured training on GMP, regulatory documentation, quality systems and technology transfer — delivered on site or remotely, scheduled around your operation.
GMP & Schedule M Readiness
What Schedule M expects of a site in practice, and how inspection findings actually arise.
2 days (indicative)Regulatory Documentation & Submissions
Building submission-grade documentation, and why applications come back with queries.
1–2 days (indicative)Quality Systems: Deviations, OOS & CAPA
Running deviation and CAPA processes that close root causes rather than paperwork.
looking for a manufacturer, not advice?
GetPharm is our verified B2B marketplace for third-party pharmaceutical manufacturing. Every manufacturer is drug-licence checked before they can list, and the enquiry, packaging spec, negotiation and payment all happen in one place.
tell us what you are working on.
Send a short description of your product, your site, or the decision in front of you. We will come back with whether we can help and what an engagement would look like.