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About
Royalmount laboratories

01

Our Progression

Our parent company Pharmascience Inc. has developed strong roots in Canada, and is Quebec’s largest employer in the pharmaceutical field with over 1500 employees.

 

Royalmount Labs external CRO business has become very successful, excelling in scientific excellence, customer service and on-time delivery. To accommodate the rapid growth, we continue to invest in the right staff, in the expansion and modernization of our laboratories, as well as in the latest technologies. 

02

Where We Are Now

Pharmascience Inc. is currently Canada’s third largest generic pharmaceutical company. 

 

Royalmount Labs now employs over 45 scientific, technical and support staff, and occupies 8000 sq ft of purpose built laboratory and office space. We have the latest state-of-the-art instrumentation including 13 LC-MS/MSs, 2 multimode spectrophotometer plate readers, a Luminex and 2 robotic liquid handling systems.

 

As a partner of choice for many pharma, biotech and virtual companies, we have a very high rate of repeat business, and this is a testament to our three core principles that we consistently deliver on to our clientele – Scientific Excellence; Customer Service; On-time Delivery. 

03

Where We’re Going

Royalmount Labs has aggressive growth plans for the next several years, including introducing new service offerings.

 

In 2023, amongst other things, we established large molecule bioanalytical and biomarker services, as well as implemented the Watson Laboratory Information Management System (LIMS). 

 

We aim to become the leading niche small and large molecule bioanalytical CRO.

Quality standards

Quality, always on time

QUALITY ASSURANCE PROGRAM

Study-based inspections (study plan, in-process, study data and report for every study and validation); additionally perform regular facility-based and process-based inspections.

COMPLIANCE WITH INTERNATIONAL REGULATIONS

Strict adherence to Health Canada, EMA, and US FDA guidelines, ensuring the highest-quality procedures, data and reports.

STRINGENT QUALITY CONTROL

Quality Assurance / Compliance Internal Auditors functions as an independent Quality Assurance Unit. 

Quality Control / Data Review Team reviews 100% of raw data generated in the bioanalytical laboratories.

  • FDA audits in 2018 (onsite) and 2022 (virtual); no FDA 483 issued
  • GLP certified by Standards Council of Canada (SCC) since 2015; most recent re-certification in 2023
  • GCP inspected by Health Canada in 2018
  • GMP inspected by Health Canada in 2020, 2022 and 2024.

Regulatory Agencies

OUR FACILITIES

State-of-the-art facilities

Our Montreal based GLP/GMP/GCP-compliant laboratories act as a key partner for numerous pharmaceutical and biotechnology companies. We adapt to the rapidly changing needs of our clients, overcoming the challenges related to regulated bioanalysis.

  • Over 45 dedicated professionals
  • 13 triple quadrupole mass specs including API 6500+ and 5000™
  • 250,000 bioanalytical samples analyzed per year
  • >300 validated assays available; extensive method development capabilities
  • 1 Shimadzu ICP-MS
  • 2 Shimadzu GC-MS/MS
  • 2 Shimadzu HPLC-UV
  • 1 qPCR
  • 2 Agilent microplate spectrophotometer readers
  • 1 Luminex
  • 2 Hamilton® STAR™

Our team

Adrien Musuku
Adrien Musuku
Senior Director, Biopharmaceutics
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Alan Bartlett
Alan Bartlett
Head, Business Development and Large Molecule Operations
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John Chapdelaine
John Chapdelaine
Director, Business Development
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Weixing Sun
Weixing Sun
Director, Research and Development
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Julien Rainville Sirois
Julien Rainville Sirois
Senior Manager, Large Molecule Bioanalysis and Biomarkers
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Babak Madadian
Babak Madadian
Bioanalytical Operations Manager
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Hong Wong
Hong Wong
Manager & Principal PK Scientist
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Ying Zhao
Ying Zhao
Laboratory Manager
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Giuseppina Vinci
Giuseppina Vinci
Manager, Quality Services
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