Own production

With more than 60 years of experience, we develop, manufacture and market a wide range of medicinal products, medical devices and food supplements for the care of women and their families. All our products undergo exhaustive quality controls.

Contract manufacturing

Backed by its extensive experience in the manufacture of medicinal products, food supplements and medical devices, since 2013 Laboratorios SEID has been offering its staff and facilities for third-party manufacturing (solid and granulated dosage forms; suspensions, solutions and semisolids, including hormonal semisolids).

QUALITY.

1 – Quality assurance

This department ensures the quality of the products manufactured at SEID by validating manufacturing processes, sanitisation and facilities, managing and supervising documentation and providing our operators with ongoing training in GMP (Good Manufacturing Practices). All sections undergo periodic internal inspections to verify compliance with the regulations. We have a CAPA management system and supplier approval protocols and external audits are performed periodically.

2 – Quality control

This department controls product quality by means of:

Sampling of raw materials and materials
Physical-chemical and pharmaco-technical testing
Microbiological testing
Validation of analytical methods/processes
Analytical transfer
Real-time and accelerated stability studies
Dissolution profiles

These two departments work together to provide effective, safe, high-quality products.

MANUFACTURING.

Authorisations

Laboratorios SEID holds a certification of compliance with Good Manufacturing Practices (GMP). We are also authorised for the manufacture, packaging, quality control, batch release and certification, storage and distribution of medicinal products, medical devices and food supplements.

We have the technology and authorisation to manufacture medicinal products for human and veterinary use, as well as investigational medicinal products, in the following dosage forms:

Solids:

tablets
coated tablets
capsules
granules
sachets

Liquids for internal and external use

Hormonal semisolids (dedicated facilities)

REGULATORY AFFAIRS.

The Regulatory Affairs department is made up of technicians with extensive experience in the sector.

This department is responsible for document management and control of registrations:

Preparation of registration dossiers in NeeS and e-CTD format.
Regulatory support from authorisation to approval of registrations (reply to allegations, etc.).
Post-authorisation regulatory work (variations, post-authorisation studies, etc.).