Accure Labs
Pharmaceutical company focused on development, manufacturing and supply of finished generic formulations with emphasis on oncology and other niche therapeutic segments. Operates multiple WHO-GMP–certified manufacturing sites in India, supports formulation and dossier development for off-patent products, and provides regulatory submission support and international distribution/partnering services across regulated and semi-regulated markets.
Industries
Nr. of Employees
small (1-50)
Accure Labs
H - 55, Sector - 63, Noida - 201307, Uttar Pradesh, India
Products
Oncology injectables
Injectable oncology formulations manufactured and supplied as finished products.
Oncology oral formulations
Oral oncology products developed and supplied as finished formulations.
Hormonal injectables and orals
Finished formulations for hormonal therapy in both injectable and oral forms.
Anti-diabetics oral drugs
Oral formulations targeting diabetic indications.
CNS oral drugs
Oral central nervous system (CNS) formulations.
Gastro-resistant oral drugs
Oral formulations with gastro-resistant/enteric properties.
Oncology injectables
Injectable oncology formulations manufactured and supplied as finished products.
Oncology oral formulations
Oral oncology products developed and supplied as finished formulations.
Hormonal injectables and orals
Finished formulations for hormonal therapy in both injectable and oral forms.
Anti-diabetics oral drugs
Oral formulations targeting diabetic indications.
CNS oral drugs
Oral central nervous system (CNS) formulations.
Gastro-resistant oral drugs
Oral formulations with gastro-resistant/enteric properties.
Services
Manufacturing of finished formulations under contract for third parties across multiple therapeutic areas.
Execution of technology transfer to enable manufacturing of developed formulations at partner or company sites.
Preparation and submission of regulatory dossiers (CTD/eCTD) and proactive regulatory intelligence tailored to target markets.
Collaborative commercial arrangements including out-licensing, distribution and marketing alliances and supply agreements.
Manufacturing of finished formulations under contract for third parties across multiple therapeutic areas.
Execution of technology transfer to enable manufacturing of developed formulations at partner or company sites.
Preparation and submission of regulatory dossiers (CTD/eCTD) and proactive regulatory intelligence tailored to target markets.
Collaborative commercial arrangements including out-licensing, distribution and marketing alliances and supply agreements.
Expertise Areas
- Finished formulation development
- GMP pharmaceutical manufacturing
- Regulatory affairs and CTD/eCTD submissions
- Contract manufacturing and technology transfer
Key Technologies
- Formulation development for oral and injectable dosage forms
- CTD/eCTD dossier preparation
- GMP manufacturing processes
- Quality control and assurance systems