lambda therapeutic research ltd
लैम्ब्डा चिकित्सीय अनुसंधान - पूर्ण-सेवा सीआरओ और बायोलॉजिक्स सीडीएमओ
लैम्ब्डा थेराप्यूटिक रिसर्च एक पूर्ण-सेवा वैश्विक सीआरओ है जो चरण I-IV नैदानिक परीक्षण प्रबंधन, फार्माकोविजिलेंस, बायोएनालिटिकल लैब और बायोलॉजिक्स सीडीएमओ सेवाएं प्रदान करता है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ahmedabad, India
- Website
- https://www.lambda-cro.com
- Categories
- फार्मास्युटिकल विनिर्माण, पूरक और कल्याण
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registry-id-verified (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registered-since (green), effective since 1998-10-27 Company Master Data (Ministry of Corporate Affairs)
- registered-address (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registry-activity (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)