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.

ADCs

 

ADCs Table

 

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.

Oligonucleotides

 

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.

Peptides

 

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:

Schedule a meeting with us to discuss your analytical needs and challenges :