lambda therapeutic research ltd
Lambda Therapeutic Research - خدمة كاملة لـ CRO والبيولوجيا CDMO
Lambda Therapeutic Research هي شركة CRO عالمية متكاملة الخدمات تقدم إدارة التجارب السريرية من المرحلة الأولى إلى الرابعة، والتيقظ الدوائي، ومختبرات التحليل الحيوي، وخدمات CDMO للبيولوجيا.
- 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
- تصنيع الأدوية, المكملات الغذائية والعافية
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)