
Antibody & TIDES Summit 2025
Amsterdam, the Netherlands
Quality Assistance will attend Antibody & TIDES summet 2025
Curious to know how Quality Assistance can help you boost the development of your Antibody-Drug Conjugates, oligonucleotides and peptides ? Meet Jordan Cossu at booth 16 during the conference!
We are experts in...
ANTIBODY-DRUG CONJUGATES
With a full analytical package for Biotherapeutics, Quality Assistance provides scientific and technical support to biopharmaceutical companies developing Antibody-Drug Conjugates.
Thanks to our combined experience with small molecule cytotoxics and monoclonal antibodies, we can provide full analytical support for your projects. We offer a wide range of services for all payload categories (maytansine derivatives, auristatins, etc.) and all conjugation strategies (lysine, cysteine, site-specific).
Throughout non-clinical and clinical development, our scientific team provides you with customised solutions in terms of analytical protocols and innovative technologies to help you move your product towards registration.

OLIGONUCLEOTIDES
Due to their relatively large size as compared to typical small molecule drugs, there are many technical challenges associated with the analysis of oligonucleotides. With a highly experienced staff and state-of-the-art premises and equipment, Quality Assistance is your partner of choice to overcome your analytical hurdles and facilitate the registration process.

PEPTIDES
Therapeutic peptides are at the crossroads of small molecules and proteins, requiring specific analytical packages depending on whether they are of recombinant or synthetic origin. Quality Assistance provides customised solutions in terms of analytical protocols and innovative technologies to help you move your peptide through non-clinical and clinical development towards registration.

QUALITY ASSISTANCE IS THE ONE-STOP SHOP FOR ANALYTICAL SERVICES
We provide:
- customised solutions in terms of analytical protocols and innovative technologies throughout non-clinical and clinical development.
- a full range of equipment in Chromatography, Mass Spectrometry, Biochemistry, Cell Biology, Pharmaceutical Technologies and Microbiology, to meet all the challenges of developing and validating methods.
- regulatory, scientific and technical excellence with a problem-solving approach
- compliance with all applicable EMA, FDA and ICH regulations
- GMP, GLP, GCLP/GCP environment
Outsource your analytical needs on one site for more efficiency including:
- Analytical development
- Validation of analytical methods as per ICH guidelines
- Characterisation of ADCs at intact, sub-unit and peptide levels
- Bioassays
- Bioanalytical services
- Stability studies
- Batch testing