Every batch leaves a paper trail — from raw material to release.

Each order moves through the same sequence, tracked at every hand-off. Nothing skips a stage, and nothing ships without a signature from Quality Assurance. 

Our R&D team profiles the chemical and physical behaviour of the API — impurity load, release profile, stability risk — and selects the excipients and process built to match. Raw materials are drawn from multiple qualified vendors, assessed against our own standards and, where required, the customer's.

Formulation development           Multi-vendor qualification         Tablets · Capsules · Sachets  

Rapid Mixer Granulators, Fluid Bed Dryers, and Octagonal Blenders run in dedicated, environment-controlled bays — tablets and capsules never share a line. Batch size sets which of our two granulation suites is used. 

RMG · FBD · OGB                      2 granulation lines           Separate tablet / capsule bays 

PLC-controlled compression machines across four stations press uncoated, film-coated, sustained-release, chewable, effervescent, and bi-layered tablets in D, B, and BB tooling. In parallel, automated fillers load hard-gelatin and vegetarian capsules to size.

Stations 27 / 35 / 45 / 61           40 lakh tablets / shift           10 lakh capsules / shift

Cores that need it move to semi-automatic coating for film or sugar coats — for taste-masking, moisture protection, or a controlled-release layer — before metal detection, de-burring, and de-dusting clear them for packing.

Semi-Auto-Coater                      Metal detection 

Light- or moisture-sensitive actives go into Alu/Alu cold-form blisters; the rest run through PVC/PVDC blister or strip packing, or loose pack for bulk orders — all on PLC-controlled lines built for export-grade consistency.

Alu/Alu cold-form                          Blister & strip                    Loose / bulk pack

Raw material, in-process, and finished samples run through HPLC, FTIR, UV-spectrometry, KF titration, and dissolution testing against IP/BP/USP or in-house specification. A separate microbiology lab clears every batch on its own protocol before QA signs release.

HPLC · FTIR · UV                    Dissolution & KF titration            Independent microbiology 

Three ICH Q1A(R2) chambers run accelerated, long-term, and intermediate stability studies across a minimum of three batches per product to set retest periods and storage claims. Regulatory Affairs compiles the dossier and clears each batch against Schedule M and WHO-GMP before it can move. 

3 ICH stability chambers                 Schedule M / WHO-GMP              Dossier & batch release 

Released stock moves through our PAN-India dealer and distributor network, direct B2B contracts with pharma companies and institutions, and Makemymeds, our own e-procurement platform — alongside export packing built for semi-regulated and regulated markets.

PAN-India distribution                     Makemymeds.com                     Export-ready packing

Two utilities sit underneath every stage above — water and air. Neither is visible in the finished product, and both determine whether it's compliant.

Feed water is chlorinated and softened before reverse osmosis strips salts, microorganisms, and organic contaminants. A mixed bed then polishes it, and UV exposure clears remaining pathogens before use.

Temperature, humidity, differential pressure, and particulate counts are set per area rather than plant-wide — because a granulation bay and a QC lab don't need the same air.