FAQs

Got Questions?

Find answers to common queries about our impurity standards, specialty chemicals, custom synthesis, and research support services.

Yes, Novapure Healthcare operates under ISO 17034:2016, ISO /IEC 17025:2017, and GMP-aligned quality systems. Our processes are driven by a team of qualified chemists and rigorous analytical validation to exceed global pharmaceutical standards.

  • We manufacture Pharmaceutical Impurity Standards, Reference Standards, GC Standards, nitrosamine impurities & Specialty Chemicals.
  • Route scouting by retro-synthesis approaches and literature survey. Enrichment of Process, leachable & Extractables impurities by degradation/isolation/purification techniques. (Preparative and flash chromatography).
  • Characterization of the unknown impurities by NMR, MS-MS, and IR.
  • Quality Assurance: ISO-compliant operations, batch-specific CoA, complete characterization data.

Yes. We provide primary-traceable secondary standards and in-house working standards. Each is fully characterized to meet the stringent documentation requirements for ANDA and DMF filings.

Every product is accompanied by a comprehensive CoA, including characterization data such as HPLC purity, 1H-NMR, Mass Spectrometry (MS), and IR spectroscopy to ensure full traceability and compliance..

Yes. Our synthesis laboratories are equipped to handle custom synthesis projects for both known and novel compounds, backed by a team capable of designing optimal synthetic routes.

Our primary focus is the pharmaceutical industry, specifically supporting teams involved in formulation development, analytical development, and generic drug research.

Yes, we have the technical capability to synthesize, isolate, and purify impurities by using preparative HPLC to their highest form from complex mixtures or API matrices.

To request a quote, please use our Online Inquiry Form or email us at admin@novapurehealthcare.com. To expedite your request, please provide the CAS Number, chemical name, or catalog number. We typically respond within 24 hours.

Lead times vary based on molecular complexity. For standard catalog items, we offer prompt shipping, while custom projects are timeline-estimated during the quotation phase.

Yes.. While our standard pack sizes are 10 mg and 50 mg, we can provide custom quantities to suit your specific analytical needs.

Yes. We are fully compliant with IATA/IMO regulations for shipping hazardous chemicals, ensuring all MSDS and UN - approved packaging are provided for safe transit.

Yes, we supply our chemical standards and impurities to pharmaceutical companies and research institutes globally, ensuring compliant packaging and documentation for international customs.

No. Our products are for laboratory research and analytical purposes only. They are not intended for human or veterinary use.

Yes, a Safety Data Sheet (SDS) is provided with every shipment to ensure safe handling and storage in your laboratory facility.

The consignment is shipped as per the shipping conditions mentioned in the Product COA.