Enter the exact COA code assigned to the analytical record.
Basel Safety Code
Controlled access to verified analytical records.
Retrieve a filed Certificate of Analysis through a unique validation code granted by your institution.
Access a certificate
🇨🇠Basel · Switzerland
Provide the authorised holder details to issue a unique Basel Safety Code.
Generate a release folio and preserve the complete access trail.
Digital certificate security
A unique code for every authorised release.
The Basel Safety Code is a unique validation folio granted by Basel Clinical Institute or by an authorised institution. It links the authorised holder, the analytical record and the permitted release in one controlled event.
The code helps prevent unauthorised access, uncontrolled forwarding and improper use of digital certificates. It is checked against the requested COA and recorded whenever access is granted.
Purity
Confirms the proportion of the intended molecular entity and monitors related substances, impurities and degradation products.
Quality
Brings identity, assay, physical attributes and specification results into a controlled analytical record.
Stability
Evaluates critical attributes under defined storage conditions and throughout the period supported by the analytical programme.
Sterility
For products intended to be sterile, compendial microbiological controls assess sterility and other applicable microbiological requirements.
Analytical framework
Methods selected for the molecule, formulation and intended use.
Peptides and related molecular products are evaluated through complementary analytical techniques. The exact test panel is defined by the specification and may include:
Identity and molecular mass
LC–MS or high-resolution mass spectrometry, peptide mapping and MS/MS sequence confirmation, as applicable.
Purity and related substances
Reversed-phase HPLC or UPLC with UV/DAD detection, supported by LC–MS when confirmation of impurities or degradants is required.
Assay and quality attributes
Validated chromatographic assay and, according to dosage form, water content, residual solvents, pH, appearance and particulate matter.
Stability
Stability-indicating chromatography under defined long-term and accelerated conditions, with trend review of degradation products and critical attributes.
Sterility and microbiological safety
Compendial sterility testing when applicable, together with bacterial endotoxin and bioburden controls where required.
Analytical procedures are selected and validated against the applicable specification, ICH Q2(R2), the European Pharmacopoeia and other relevant compendial requirements.
Secure document access
Locate a Certificate of Analysis.
The document is released only after the certificate and authorised holder information have been validated.
Release traceability
One Basel Safety Code. One authorised release record.
The access model is centralised around a single validation code. The code is unique, linked to an authorised holder and checked against the requested analytical record.
Code assignment
The institution grants a unique Basel Safety Code for the authorised certificate scope.
Holder validation
The holder name, email and Basel Safety Code are checked before the document is released.
Release record
Every successful consultation generates a separate release folio with the requester, certificate, date and validation code.