International Standards

World Class Dedicated manufacturing facilities for formulations as well as APIs further exemplify our expertise in manufacturing variety of dosage forms . All manufacturing sites are WHO-GMP approved and new state-of-the-art manufacturing facilities are applied for registration at USFDA, UKMHRA and TGA-Australia.
Our state-of-the-art manufacturing facilities have following salient features:

• Fully computerized Heating,Ventilating and Air-conditioning System (HVAC).
• Production area made of sandwich panels & self-leveling PVC flooring.
• Validation Master Plan (VMP) as per European GMP 2002 and CGMP 210 & 211.
• Modern QA, QC, Microbiological and PD Lab supported with high-tech equipments.
• Fully automated with electronically controlled operating system as per GAMP-4 (Good Automated Manufacturing Practice) guidelines.
• Sophisticated Effluent Treatment Plant (ETP) with the capacity of 100000 Ltrs/day making it environment friendly company.
• Built to conform international environmental, health & safety regulations.

1. Oncology Unit dedicated to manufacturing of our leading anti-cancer formulations
   Lyophilization
   Sterile - Liquid Ampoule / Vial, Dry Powder
   Tablets & Capsules

2. Hormones Unit dedicated to manufacturing the highly purified hormonal preparations such as Gonadotrophins
   Lyophilization
   Sterile - Liquid Ampoule / Vial
   Tablets & Capsules

3. General Formulation Unit, dedicated to manufacturing of various dosage forms including other critical care and cardiovascular formulations
   Lyophilization
   Sterile - Liquid Ampoule / Vial, Dry Powder
   Sterile Ophthalmic Formulations
   Tablets, Capsules And Syrup
   Soft Gelatin Capsules
   Aerosols

4. Cepahalosporin Unit , further divided into 2 separate facilities :
   i}Cepahalosporin facility specialized in manufacturing of lifesaving cephalosporin formulations for
   Injectables
   Tablets & Capsules
   ii}Beta Lactam facility, specialized in manufacturing of lifesaving antibiotics as
   Oral Solids
   Injectables

Click here to see API`s.



Stringent Process Norms

VHB Life Sciences Inc. believes in the philosophy of Brand Building and this belief results in its deep commitment to product quality. At VHB Life Sciences Inc., quality is not by mere chance, but is the result of systematic and intelligent work.

The pedestal on which product quality at VHB Life Sciences Inc. benchmarks itself, is stringent adherence & follow up of standard protocol involving approved procedures, production planning and control process with complete documentation.

All procedures of Quality Control follow stringent in-process checks at every stage leaving nothing to chance. Documentation is carried out for every process resulting in more than adequate record of each and every data generated.

In compliance with cGMP norms, the entire manufacturing is spearheaded keeping close eye on national & international regulatory norms and more importantly our client's customary requirements.