COSMETIC FIELD

Analysis of the safety of cosmetic products in compliance with the requirements established in Regulation 1223/2009 of the European Parliament and of the Council.

Efficacy studies of cosmetic products.

Certification in compliance with ISO 22716 (good manufacturing practices of cosmetic products) through the accredited certification body.

VALIDATION AREA

Validation of all types of process Pharmaceutical, Cosmetic, Food sectors.

Pre regulatory inspeciton audits

Validation of Machinery and Installations for pharmacy, cosmetics or food sector.

Software validation

Advice on regulatory issues in pharmaceutical / cosmetic sectors

Second and third part audits, internal audits and to suppliers.

Pharmaceutical scope

GMP, GLP, GDP

Training

Equipment qualification

Medication registration

Processing of licenses with international health authorities

Bibliographic review of product files

WHO WE ARE SERVICES TECHNICAL INSPECTION

Our services

INTERCER audits and certifies quality management systems and medical devices for conformity with ISO 13485 and compliance with European regulatory requirements for medical devices as well as national laws. It exclusively certifies medical devices and healthcare products.

Due to a high level of in-house expertise and competence, we are able to certify even highly innovative and complex devices as well as drug-device combinations.

INTERCER services include:

Certification according to ISO 13485

Validation of computer programs according to pharmaceutical industry requirements

Audits and certifiction under GDP scheme

Certification represents a strategic decision for pharmaceutical industry and secures them competitive advantages within the regional and the international markets. The introduction and certification of a quality management system offers the possibility of optimally increase potential with regards to management organisation, productivity and customer satisfaction.

The audit is carried out by our experts with extensive industry experience