ALS Scandinavia has a GMP certificate, GLP statement of compliance and is approved by the FDA (reference no. FEI 3007165135). Furthermore it is ISO 170 25 accredited.
ALS Scandinavia is regularly audited by pharmaceutical companies and participates in various inter-laboratory comparison programs on a routine basis. ALS Scandinavia has performed more than 100 client-specific method validations to the pharmaceutical industry. As your partner, we will meet all your requirements from sample handling to confidential information management.