Science, precision and integrity — from plant to patient
An India-based, MSME-registered pharmaceutical company focused on the development, manufacture, import–export and commercialisation of high-purity APIs derived from herbal and botanical sources.
Positioning India as a leader in pharma-grade herbal APIs
Incorporated under the Companies Act, 2013 and established in 2024, Chemicraft is on a mission to combine traditional phytochemistry with cutting-edge extraction and purification technology.
The Company develops, manufactures, imports, exports and commercialises Active Pharmaceutical Ingredients, herbal extracts, nutraceutical actives, advanced intermediates, impurities, pellets and finished formulations. It has already secured its Drug Trade Licences from the Government of Haryana and holds the key regulatory identifiers required for domestic and export operations.
Our proposed greenfield facility at Adampur, Hisar is designed to international GMP standards and will produce nicotine APIs, herbal botanical extracts, licorice-derived actives, Vitamin D3 and cosmetic-grade nutraceutical actives — targeting the global API market, estimated at USD 245 billion.
We aspire to be recognised worldwide as a reliable, trusted Indian partner offering superior quality, competitive pricing and consistent service.
Vision
To be the world’s most trusted manufacturer of pharma-grade herbal APIs, delivering nature’s therapeutic potential through science, precision and integrity.
Mission
To establish a GMP-certified, technology-driven manufacturing facility that produces high-purity botanical APIs for global markets, while championing sustainability, innovation and India’s pharmaceutical self-reliance.
What we stand for
Quality First
Every batch meets or exceeds pharmacopoeial standards — USP, EP, IP, BP.
Scientific Integrity
Data-driven decisions, validated processes and transparent documentation.
Sustainability
Zero Liquid Discharge facility and green extraction methodologies.
Patient Focus
Our APIs ultimately serve patients globally — quality is a non-negotiable duty.
Innovation
Continuous R&D in yield improvement and novel extraction techniques.
Compliance
Strict adherence to Schedule M, WHO-GMP, ICH Q7 and global regulatory norms.
- Quality Excellence
- Compliance by Design
- Scientific Rigor
- Sustainability
- Transparency
- Long-term Partnerships
- Ethical Conduct
Experience that has built plants, licences and global supply chains
A management and technical team with 100+ years of combined pharma experience across API plants, formulation units, exports and regulated markets including the US, EU and Japan.
Strategy, Business Development & Marketing
Drives the strategic vision and commercial direction; oversees marketing, customer acquisition, partnerships and investor relations.
- 30+ years in international marketing and brand management
- Post-graduate qualifications in Management and Digital Business
- Deep understanding of herbal API export markets across USA, EU and Asia
Legal, Regulatory Compliance & Governance
Responsible for legal, regulatory and compliance functions, including drug licensing, CDSCO / Schedule M frameworks, IP protection and the ESG policy.
- 22+ years in pharmaceuticals and FMCG
- Regulatory filings, international audits, quality and EHS/ESG policy
- Legal affairs, litigation, arbitration, land, IPR and taxation
Operations
Leads plant operations, supply chain, vendor management and production planning from greenfield commissioning to steady-state production.
- 30+ years in pharmaceutical and food manufacturing
- Managed projects worth over INR 1,000 Cr
- Expertise in EcoVadis, CDP and SBTi sustainability frameworks
Engineering, Projects & Infrastructure
Oversees engineering and infrastructure for the Adampur facility: plant design, extraction and distillation equipment, utilities, ETP/ZLD.
- 35+ years handling large projects; Mechanical Engineer, IIT
- Managed projects worth over INR 700 Cr
- Detailed mechanical, electrical and civil plant engineering
A specialist team behind every function
Nine functional heads, each with 10–15+ years of experience, supported by chemical engineers, process technologists, formulation scientists and senior validation consultants.
Manufacturing
Plant operations, production planning, capacity utilisation, GMP compliance
Quality (QA & QC)
GMP compliance, USFDA / WHO / AYUSH readiness, batch release, CAPA, vendor qualification
Research & Development
Herbal extract standardisation, Vitamin D3 process development, DMF documentation, tech transfer
Regulatory Affairs
USFDA / EU filings, DMF / ANDA preparation, AYUSH registrations, export documentation
Supply Chain
Raw-material sourcing, vendor development, inventory planning, logistics & imports
Engineering
Utilities, preventive maintenance, equipment installation, project expansion
Finance & Commercial
Costing, working capital, banking & LC, export finance, investor reporting
Sales & Business Development
Global API sales, herbal-extract clients, contract manufacturing, distributor network
Environment, Health & Safety
Pollution compliance, hazardous-chemical safety, worker safety, ETP operations
Meet the team behind the plant
Discuss supply, co-development or investment with our leadership.