FINISHED FORMULATION

With the combined vision and long-term view, Accuris entered finished product business and established its own brands in India market in area of Diabetics, Cardiology, Hypertension, Genecology, multi-vitamin, Hormone and steroid. Since inception, we have been focusing on chronic and lifestyle related therapies with a strong focus on high-end super-specialist doctors and consulting physicians.

We specialize in licensing / out licensing projects on behalf of our extensive range of partners and principals based in India. We have wide range of finished products in various therapeutic segments to offer for export market Through our partners and alliances, we can offer Formulation Development and Contract Manufacturing with complete regulatory support. Accuris exports finished products to various countries under own brands and undertaking registrations with local regulatory agencies in Africa, Middle east, Asia, CIS and Latin American region.

ACTIVE PHARMACEUTICAL INGREDIENTS

Considering long term view, we're engaged in Contract Manufacturing of APIs & Advance Intermediates, Contract Manufacturing is done mostly on a product exclusive basis.

Apart of our own APIs and Intermediates, Accuris supplies and sources an extensive range of Bulk Active Pharmaceutical Ingredients, Intermediates, Nutraceuticals from WHO, cGMP, EUGMP and FDA approved plants.

Accuris partners with many manufacturing companies who keeps on developing new products which can be made available to customers for early-stage development to grab the market.

Through our manufacturing partners and alliances, we can offer custom synthesis and Contract Manufacturing with complete regulatory support. Accuris helps Active Ingredient and intermediate manufacturers to have them an access to the global markets.

TECHNICAL SERVICES

GMP audit services for Active Pharmaceutical Ingredients, Excipients, packaging materials, Key Starting Materials and Intermediates through experienced and certified GMP Auditor

Sourcing of suitable third-party vendor audit reports of suppliers located globally Good Distribution Practice audits for Transporters at Freight forwarders, Ground transportation, Sea line and Air Cargo complex Good Manufacturing Practice consultation related services into green field projects and Brown field projects, Implementation of Quality Management System, Data Integrity issues remediation projects, Gap/Risk assessment projects at manufacturing site of Finished formulations, Active Pharmaceutical Ingredients, Excipients, Packaging materials, Key Starting materials and Intermediates.

Complete automation and validation services in QA, QC and manufacturing area.

Development of inhouse software for audits (internal/external) and observation tracker

Development and Implementation of cost saving software related to Training management system, Management review meetings, Change control, CAPA, deviations and Market complaints.

Development and Implementation of document management system to maintain SOPs, Validation protocols and report, Qualification documents (FDA part 11 compliant), User access management system (can be integrated to LIMS)