INTERCER NORTH AMERICA: EXPERTS IN MANAGEMENT
Our pharmaceutical services are dedicated to help you to overcome the challenges of drug development and manufacturing.
With Intercer North America as your partner, you can trust us to provide
The quality and technical requirements for medical facilities and equipment are becoming stricter all the time. We can keep your company in tune with day-to-day requirements.
Strategically using certifications
With the INTERCER North America services, pharmaceutical industry can benefit from the advantages of certification as per ISO 9001 or ISO 13485 – as quality and competence in pharmaceutical industry are important competitive advantages.
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.
Existing cooperations are secured and access to future cooperations with partners and other service providers within the health sector is also made easier.
The audit is carried out by our experts with extensive industry experience – therefore, they speak the language of our customers.
Existing quality, environmental and occupational safety management systems, etc., can be combined
INTERCER NORTH AMERICA SERVICES:
In order to provide a competitive service that provides added value to manufacturing companies, THREE potential areas of collaboration in the field of cosmetic products have been developed:
Analysis of the safety of Cosmetic and Medical products in compliance with the requirements established in current legislation (for example Regulation 1223/2009 of the European Parliament and of the Council).
Efficacy studies of cosmetic products and health products.
GMP Audits
GLP audiotis
GDP audits and certification under EU directive.
Certification in compliance with ISO 22716 (Good Manufacturing Practices of Cosmetic or Sanitary Products).
Certification in compliance with ISO 13485
Informatic service Validation
Compliance certification / audit
Facilities inspection
Certification, inspection and audit solutions focused on business optimization.
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
CONFIDENCE
SECURITY
FLEXIBILITY
NOTE: THIS WEBSITE DOES NOT USE COOKIES OR ANY MEANS OF VISITOR CONTROL.
244 Fifth Avenue, Suite 1203, New York, NY 10001 US
