The Company
V.S. Interchem Private Limited was incorporated in 2003 and is based in New Delhi, India. A turnkey execution company that designs, equips, installs, qualifies and documents complete pharmaceutical manufacturing facilities.
Most pharmaceutical plants are built by engineering contractors who have never manufactured a medicine.
We have built four for our own account, and then had to operate them.
Our Own Account
Not projects we handed over and walked away from. Plants we then had to staff, run, maintain and put through inspection ourselves. Every constraint a working facility imposes, from cleaning access to material flow at shift change, to where a deviation gets recorded, to what an auditor asks for and how fast it can be produced, we have met from the inside. That experience is what we design with.
In House
A turnkey contract only means something if the functions it depends on sit inside the same organisation. Ours do.
Layout, flow, civil, structural, MEP, HVAC and utilities design carried through from concept to issued-for-construction drawings.
Specification, vendor qualification and contracting for equipment, with the company purchasing as principal.
Programme, sequencing, site coordination and the single reporting line the client deals with.
Practical manufacturing input into layout and equipment selection, drawn from operating our own units.
Quality management system, standard operating procedures and the documentation set that accompanies the plant.
Laboratory design, analytical method transfer and the specification of QC and microbiology functions.
Dossier and CTD compilation, product registration and regulatory strategy for the target market.
Leadership
Director
Three decades in the pharmaceutical industry, spanning formulation manufacturing, pharmaceutical machinery and the delivery of turnkey facilities. He has led the establishment of the company's own formulation units in India and its international project execution.
Director
A chemical engineer by training, bringing process and engineering discipline to the company's international projects. He leads project development and client engagement, including regulatory strategy and market-entry planning.
Director, Regulatory Affairs
Leads the regulatory affairs function, covering product registration, dossier compilation and regulatory compliance across international markets.
Credentials
Facilities designed and documented to WHO-GMP and EU-GMP standards.
Group registered with Pharmexcil, the Pharmaceuticals Export Promotion Council of India.
Tell us the dosage platforms you are considering, the market you are registering in and the status of your site. We will tell you what the project actually involves.
