01
APIs & intermediates
Second-source APIs for EU generic manufacturers, with the CEP or ASMF route identified before you ask for a sample.
Ibuprofen · Losartan potassium · Levetiracetam · Omeprazole
See APIsEU gateway for Indian pharmaceutical ingredients · Poznań
Sourced in India.Accountable in Europe.
APIs, botanical raw materials and specialty chemicals from qualified Indian manufacturers, with every document checked against EU requirements by a Polish team that stays your single point of contact.
57–70%
of valid CEPs for ibuprofen, losartan, levetiracetam and omeprazole are held by Indian manufacturers.
EDQM CEP database, valid on 15 Oct 2026; GFC count
72.6%
of the EU’s turmeric imports from outside the EU came from India in 2025, by value.
Eurostat Comext, CN 0910 30 00
10%
of consignments of Indian botanical food-supplement ingredients are checked at the EU border, with an official certificate and lab report for ethylene oxide.
Reg. (EU) 2019/1793, Annex II, as amended by 2026/1206
What we supply
Four product groups, checked to the same document standard.
We focus on ingredients where Indian manufacturing is strong and EU documentation decides the deal.
02
Botanical raw materials
Psyllium, curcumin, boswellia and mint oils, specified to your requirements, with contaminant data for every batch.
Psyllium husk 99% · Curcumin 95% · Boswellia serrata extract · Peppermint oil
See botanical raw materials
03
Private-label formats
Gummies, oral strips, tablets and powders for EU brands, with label, notification and claim checks built in.
Gummies · Oral thin films · Tablets · Powders
See private-label formats
04
Cosmetic & industrial chemistry
Castor derivatives, solvents, surfactants and gums in full-container lots, with SDS and REACH information.
Hydrogenated castor oil · Ethyl acetate · SLES 70% · Guar gum
See chemicalsThe documented route
Five checkpoints between an Indian plant and your goods-in.
Price comes last. First we make sure the paperwork will survive your QA review.
- 01
Source
We shortlist manufacturers that already supply the EU: valid CEP or ASMF, inspections without critical findings, export experience.
- CEP / ASMF status
- EudraGMDP record
- 02
Qualify
Questionnaire, certificate checks in official registries and, where the product requires it, an audit before the first order.
- Quality questionnaire
- Audit report
- 03
Document
We assemble the package and review it against your specification and EU rules before we send a quotation.
- Specification & CoA
- Written Confirmation
- Nitrosamine & ICH Q3D statements
- 04
Import & test
EU import, customs and border controls. For botanicals we require accredited-laboratory results for ethylene oxide, pesticides and heavy metals for every batch.
- Import documents
- Test reports
- 05
Deliver
Until our own GIF registration is in place, active substances will be imported and delivered through a licensed Polish partner (agreement in negotiation), named in each offer. We remain your single contact for documents and questions.
- Offer naming the licensed partner
- Batch documentation
Ingredient index
Every ingredient, with its CAS number.
Each ingredient has its own page with CAS number, pharmacopoeial grade, typical packaging and the documents we can provide. Not on the list? Send us the specification.
| Ingredient | CAS | → |
|---|---|---|
| IbuprofenIbuprofenum · (RS)-2-[4-(2-methylpropyl)phenyl]propanoic acid | 15687-27-1 | |
| Losartan potassiumLosartanum kalicum · Losartan K | 124750-99-8 | |
| LevetiracetamLevetiracetamum · (2S)-2-(2-oxopyrrolidin-1-yl)butanamide | 102767-28-2 | |
| OmeprazoleOmeprazolum | 73590-58-6 | |
| Psyllium husk (Plantago ovata)Ispaghula husk · Plantago ovata Forssk. seed husk | 8063-16-9 | |
| Curcumin 95% (turmeric extract)Curcuma longa L. rhizome extract · Turmeric extract (CAS 84775-52-0) | 458-37-7 | |
| Boswellia serrata extractIndian frankincense extract · Boswellia serrata Roxb. gum resin extract | 97952-72-2 | |
| Peppermint oil (Mentha × piperita)Menthae piperitae aetheroleum · Mentha piperita oil | 8006-90-4 |
Who does what
Clear responsibilities, from the plant to your QP.
Your QA team needs to know who is accountable for each step. This is how the work is split.
ResponsibleSupports or checks
| Manufacturer (India) | Licensed partner (PL) | Green Future Clinics | You | |
|---|---|---|---|---|
| Manufacturing, GMP and batch release | Responsible | — | — | — |
| CEP or ASMF and EU GMP certificate | Responsible | — | Supports or checks | — |
| Written Confirmation (issued by CDSCO) | Responsible | — | Supports or checks | — |
| Document pre-check before quotation | — | — | Responsible | — |
| Supplier approval and qualification (your QP) | Supports or checks | — | Supports or checks | Responsible |
| Import of active substances (GIF-registered importer) | — | Responsible | — | — |
| GDP storage, transport and supplier verification | — | Responsible | Supports or checks | — |
| Accredited-lab results for botanicals (EtO, pesticides, metals) | Supports or checks | — | Responsible | — |
| Commercial terms and single point of contact | — | — | Responsible | — |
| QP certification of your finished product | — | — | — | Responsible |
Until Green Future Clinics is entered in the GIF register of active-substance importers, imports of active substances will be handled by a licensed partner (agreement in negotiation), named in each offer. Supplier approval always remains with your Qualified Person.
Transparency
Where we are today.
We are a young company. Rather than borrow badges, we show our status. This list is dated and changes as we progress.
- 01Sourcing network in IndiaActive
Through Sudarshan Pharma Industries; we shortlist manufacturers that already supply the EU.
- 02Documentation reviewActive
CEP/ASMF, GMP, CoA and Written Confirmation checked before quotation.
- 03Licensed Polish partner for active substancesIn progress
Agreement in negotiation. Imports of active substances will run under the partner’s GIF registration.
- 04Own GIF registration as active-substance importerIn progress
In preparation, with a quality system that follows EU GDP for active substances. We publish the filing date here.
- 05Accredited laboratory partnerIn progress
Selection in progress. Until signed, we require results from the manufacturer’s ISO/IEC 17025-accredited laboratory.
- 06Packaging & labelling in PoznańPlanned
Planned for private-label supplements.
Last reviewed:
Insights
Written for QA and procurement.
APIs · Regulatory · 7 min read
CEP or ASMF? How API documentation works in EU generic dossiers
A CEP is an EDQM certificate confirming that the Ph. Eur. monograph controls one manufacturer's substance. An ASMF is a confidential file the authority assesses with each application. Both support Module 3. Neither replaces the buyer's own checks on GMP, impurities and import papers.
Read moreBotanicals · Food safety · India · 7 min read
Ethylene oxide in Indian botanicals: what EU buyers test for in 2026
Ethylene oxide residues are measured as the sum of ethylene oxide and 2-chloroethanol. EU limits sit at the limit of quantification. As of October 2026, many Indian spices and botanical food-supplement ingredients still need an official certificate and lab report at the EU border.
Read moreAPIs · Regulatory · India · 7 min read
Buying APIs from India: the EU document checklist
An API from India needs evidence of EU GMP, a CEP or ASMF, and a written confirmation from India's regulator. Each batch needs a specification and certificate of analysis. In Poland, the importer registers with GIF and follows EU GDP for active substances.
Read more
Send us your molecule list.
Tell us what you buy, in what volume and which documents you need. We aim to reply within one business day with availability, documentation status and next steps.
Or write to hello@gfclinics.pl