Serving Contract Manufacturing Organizations (CDMO/CMO)
CDMOs and CMOs sit in a tricky spot — they're accountable to their own clients' formulation specs, timelines, and regulatory filings, all while depending on raw material suppliers they don't fully control. That makes supplier reliability less of a preference and more of an operational necessity. One inconsistent shipment doesn't just affect one batch — it can ripple across every client project running through that facility.
We act as a consolidated single-source raw material vendor for contract manufacturers, offering bulk APIs (Lidocaine Base & HCl), synthesis intermediates (2-Chloro-2,6-dimethylacetanilide), and pharma-grade solvents (IPA, MDC, Acetone, Ethyl Acetate, DMSO, NMP). Sourcing multiple compliant materials under one umbrella simplifies supply chain logistics, reduces vendor qualification friction, and speeds up tech-transfer timelines.
Our production facilities in Ankleshwar, India operate under WHO-GMP, cGMP, and ISO 9001:2015 certifications. With complete Drug Master File (DMF) packages, comprehensive Certificate of Analysis (CoA) documentation, and flexible order scaling from pilot batches to commercial metric tons, Alex Pharmachem gives CDMO partners the reliability needed to fulfill contract deadlines seamlessly.
General Information
Contract manufacturing and development organizations produce pharmaceutical products on behalf of other companies, often juggling multiple client formulations, specifications, and regulatory pathways simultaneously. Unlike a manufacturer producing a single in-house product line, a CDMO's raw material needs shift project to project — which puts a premium on suppliers who can deliver consistent quality across a broad but well-defined range, rather than suppliers who only do one thing well.
That's where our portfolio structure tends to fit naturally. The company also provides finished actives such as Lidocaine APIs (Base & Hydrochloride), Chlorhexidine, and its derivatives. Our company also provides a wide range of solvent products that include IPA, Acetone, Ethyl Acetate, Glacial Acetic Acid, Chloroform, Methylene Chloride, Benzyl Alcohol, DMSO, NMP, Glycerine, and PEG. For a CDMO running multiple client formulations, sourcing several raw material categories from one qualified supplier meaningfully simplifies vendor management and documentation overhead.
Certification Backbone
Every product in our range carries the same certification backbone — WHO-GMP, FDA, Written Confirmation, HALAL certification, ISO 9001:2015, ISO 14001:2015, ISO 45001:2018, and Open & Closed Part DMFs.
This matters considerably to CDMOs, since documentation gaps on a raw material can stall a client's regulatory submission just as easily as a quality issue can.
Why Choose Us
Broad, relevant product range under one roof
APIs, solvents, and intermediates, reducing the number of suppliers a CDMO needs to manage
Documentation built for regulatory pass-through
DMFs and certifications that CDMOs can reference directly in client filings
Flexible order scaling
capacity structured for both trial-batch and long-term commercial supply, matching how CDMO project pipelines actually move
Two decades of manufacturing consistency
since incorporation in 2000
Single point of contact across multiple raw material categories
cutting down vendor coordination time on multi-client projects
Applications
CDMOs and CMOs typically source from us for:
Client Anaesthetic & Antiseptic Projects
Client projects centered on local anaesthetic or antiseptic formulations, using our Lidocaine or Chlorhexidine APIs.
Process Solvents Workflows
Process solvents needed across a range of client synthesis and purification workflows.
Pharmaceutical Intermediates Sourcing
Pharmaceutical intermediates required for in-house synthesis of client-specified compounds.
Multi-Product Consolidation
Multi-product sourcing where consolidating suppliers reduces administrative and qualification overhead.
