About Us

Material & Solvent handling Practice

• We are following Standard Procedure for Raw material and finished product Identification & Labelling, Handling and Storage.

• We have a Separate Ware-house From Company Premises to Store the Material and Solvent.

• Well Defined SOP For Solvent handling and Storage as per their Compatibility.

Manufacturer And Dispatch

• We Processed Work in Flash column system for Isomer separation,

• We also working on Phytochemicals purification and concentration enrichment by Column Chromatography at Lab Scale Trials.

Quality Policy-EHS Policy

• Our Quality and EHS policies prioritize continuous improvement and compliance, ensuring the highest standards of product quality and environmental health and safety across all operations.

• Ensuring the Quality and EHS is our priority, as reflected in our comprehensive Policy, which outlines our commitment to excellence.

• Well defined and established Risk Assessment system Like SWOT Analysis & Context analysis & Risk assessment.

• Recently EHS system is audited by our customers Dishman Carbogen Amcis Ltd. And Torrent Pharmaceuticals Ltd.

• Our Quality Policy align With ICH Q7 Guideline for good manufacturing practice for the manufacturing of active pharmaceutical ingredients (APIs).

• 20 floor persons are Trained & Certified from Fire institutes in “FIRE & SAFETY” Programme.

KEY STRENGTH

At Aarpan Remedies LLP, we specialize in contract research and manufacturing for the pharmaceutical industry, offering end-to-end solutions from R&D to commercial production. Our GMP-certified manufacturing facility in Chhatral, Gujarat, ensures compliance with global quality standards, delivering high-quality pharmaceutical intermediates and APIs. With a strong R&D-driven approach, we focus on innovation, process optimization, and rapid scale-up, enabling seamless technology transfer and cost-effective manufacturing. Our customer-centric approach ensures tailored solutions, while our commitment to sustainability and ethical practices drives responsible manufacturing. By integrating cutting-edge technology, stringent quality control, and regulatory compliance, we strive to be a trusted partner for pharmaceutical companies worldwide.

Safety by design manufacturing site

• Plant designed keeping safety first in the design concept. Having well ventilated equipment and process area, well designed escape route in case of any Emergency.

Zero carbon footprint mission

• Being responsible to beloved mother nature and with our working standards of being conscious of our existence, we will be Zero carbon foot print company in next 10 years, operating at carbon neutrality via Tree plantation and energy generation via waste. Will be planting more than 2 millions plants in the surrounding community.

Experience of CRO

• With the experience of CRO of almost 10 years, We are aware of the critical requirements of the customer.

APPROVALS

• Environment Clearance for the project from state pollution control board

• No objection Certificate from state pollution control board

• FDA license from food and drugs department for manufacturing of API

• FIRE NOC from fire & Safety Department

• License for usage of various solvents from regulatory authorities

Certifications

• ISO 9001: Quality Management system

• ISO 14001: Environment Health & Safety

• ISO 18001: Occupational Health and Safety Assessment

QUALITY ASSURANCE

• Well established quality assurance system as per ICH Q7 guidelines.

• Elaborate list of Standard operating procedure for all components of the operations.

• Proper training and record on SOP/Format filling/Safety Etc.

OTHER DETAILS

• Strong R&D Team for handling of any type pf chemistry and scale up.

• Strategic partnership with outside quality control lab (USFDA approved) for third party testing of every final material manufactured.

• Having all Govt. as well regulatory compliance for running a chemical company.