We pride ourselves on offering a comprehensive range of services in
Biosciences & Pharma
Here at Sciom Limited, we are dedicated to providing a comprehensive range of services to the pharmaceutical and biosciences industry. Our team of experts are committed to delivering exceptional service and tailored support to meet the individual needs of each client.
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About
SCIOM Limited
Founded in 2023, we hold over 20 years of experience in quality control, specialising in the development and validation of chemical/physical analysis, microbiological testing, and biological testing in alignment with current ICH and EU GMP guidelines.
Our team has collaborated with a variety of companies, including start-ups and established enterprises, on a wide range of projects encompassing business development, clinical development, quality control, quality assurance, qualified persons, regulatory affairs, and more.
WHY CHOOSE US
At Sciom, quality serves as the cornerstone of our operations, driving every aspect of our activities. We are deeply committed to upholding the highest standards of quality, a commitment that involves the active participation of all employees across every level of the organisation. Our objective is to consistently elevate the quality and integrity of our products to the utmost standards. To achieve this, we have implemented robust quality systems that adhere to Good Manufacturing Practices. These systems form the foundations of our quality policy, ensuring that our products consistently meet and exceed regulatory requirements while also exceeding the expectations of our valued clients.
Service &
Solution we
provide
At Sciom Limited, we are dedicated to providing a comprehensive range of services to the pharmaceutical and biosciences industry.
CDMO Services
Development activities include early stage formulation and Analytical development, Technology transfer, scale-up, process validation and stability testing...
Regulatory Services
Our Scientific writing professionals are provided as an incorporated part of our clinical development expertise or as a standalone...
Audit Management
In the pharmaceutical industry, ensuring compliance with Good Manufacturing Practices and Active Pharmaceutical Ingredient regulations...
Pharmacovigilance
Safety is an essential ingredient of any clinical studies. Pharmacovigilance is like a sunshade to represent activity for continuous monitoring...