Manufacturing & Quality

Quality-Driven Manufacturing Through Certified Partners

We partner with reputed, independently audited contract manufacturing sites that are WHO-GMP certified, ISO certified, and approved by various other reputed regulatory agencies. This model allows us to focus on formulation development, quality oversight, and partner service while our certified manufacturing partners produce every batch under stringent, globally aligned quality systems.

Our partner manufacturing sites are equipped to produce a wide range of dosage forms, including creams, gels, syrups, softgel capsules, hard capsules, tablets, and inhalation solutions. Each facility maintains validated production lines, controlled environments, and documented standard operating procedures aligned with WHO-GMP and Indian pharmacopeial requirements. Environmental controls govern temperature, humidity, and particulate levels, while dedicated cleanroom zones prevent cross-contamination between product families.

Quality assurance is embedded across the entire product lifecycle. Each batch is accompanied by complete certificates of analysis and characterization documentation, confirming composition, identity, and purity through orthogonal analytical techniques — including HPLC, GC, UV spectrophotometry, and dissolution testing. Stability studies monitor product performance across shelf life, ensuring that patients receive medicines that remain safe and effective from manufacture to last use.

To further reinforce confidence in every product, our CMO conducts comprehensive in-house testing on each batch and additionally provides samples to independent external laboratories for third-party verification. This dual-layer testing approach — internal quality control validated by external analysis — provides an added layer of assurance, reassuring both partners and patients of the safety, purity, and consistent quality of every Novamedrex formulation.

Novamedrex also offers custom formulation development for partners with unique requirements, leveraging our scientific expertise and our network of certified manufacturing sites. Whether developing a new dermatological skincare line, a respiratory syrup, or a nutraceutical supplement, our team works closely with partners from concept through commercialization — delivering reliable, high-quality medicines that healthcare providers and patients can trust.

Certified contract manufacturing facility producing pharmaceutical formulations under controlled conditions

Certified Partners

Our formulations are produced by reputed contract manufacturing sites that are WHO-GMP certified, ISO certified, and approved by various reputed regulatory agencies — ensuring every batch meets global standards for safety, efficacy, and consistency.

Analytical research laboratory confirming pharmaceutical composition and purity

Analytical Research

Light through glass — our analytical research confirms structure, identity and purity through orthogonal techniques. Complete characterization data accompanies every batch, smoothing the path to regulatory approval.

WHO-GMP Certified Sites
Products manufactured at WHO-GMP certified contract manufacturing facilities.
ISO & Regulatory Approved
Partner sites approved by ISO and various reputed regulatory agencies.
Multi-Formulation Capability
Creams, gels, syrups, softgels, capsules, tablets, and inhalations.
Orthogonal Characterization
Composition and purity confirmed by multiple analytical techniques.
Complete Documentation
Certificates of analysis and stability data for every batch.
Dual-Layer Testing
In-house CMO testing plus independent external lab verification for added safety assurance.
Custom Formulation
Bespoke formulations developed to partner specifications, on demand.