Pelmy Science Cyprus (PSC). Research & Development Center

An organization,  that provides services to over 15 countries and  international pharmaceutical companies.

Our main objective

To provide pharmaceutical research and development services tailored to our clients’ needs.

PSC R&D Center, offers full product development services to generic pharma companies and specialty pharma focused on the development of new improved versions (value-added generics or generic plus) of established drug products. Typically, our clients approach us with a specific development request but occasionally, we are also asked to investigate and propose new product opportunities based on the existing drug portfolio of our clients. Although in general the overall aim of value-added generic development projects is focused on improving the safety, efficacy and/or the ease of administration, we are also specialized in executing development programs where the primary or sole objective is the evasion of existing product patents.

Thanks to our wide range of services, our high-performance equipment ,  a strict quality control system and our worldwide collaborators we can offer efficient solutions within set deadlines.

Our Team

Our organization has a team with extensive experience in analytical, formulation, manufacturing and regulatory activities in the R&D pharmaceutical field.

PSC has wide experience and capacity for all kind of development projects, from generic to innovative drugs, from simple to complex products, including the ability to handle highly potent compounds. It also offers innovative solutions and our goal is more safe and more excellence products.

PSC state of the art GMP-compliant, high containment facility is equipped to develop and monitor manufacture high potency products, specializing in the development and management of such products.

From initial pre-formulation trials up until monitoring commercial manufacturing, PSC provides all relevant activities during the lifecycle of a pharmaceutical product.

Client Focused

PSC does not have its own pharma product portfolio, preferring to focus solely on providing services to its client base, offering agile, flexible and qualitative services to clients, and meeting the deadlines required for each project.

PSC state of the art GMP-compliant, high containment facility is equipped to develop and monitor manufacture high potency products, specializing in the development and management of such products.

We value your feedback as we are committed to continuously improving our products and services with the appropriate consistent Quality, Reliability and Safety for the purpose for which it is intended.

With costumer focus is a strong contributor to the overall success of our business and involves ensuring that all aspects of the company put its customer’s satisfaction first.

Our Ethics Base

Carve a niche on the global map through traditional wisdom and values and repose the faith of our customers, staff and shareholders.

Our procedure. Focus on compliance framework.

Reliable and reproducible analytical methods are essential to both the pharmaceutical development and the evaluation of pharma product to meet the defined Industry Standards of potency, purity and stability.

Analytical chemists work to develop, qualify and validate or refine analytical methods to meet these demands.

We have multisite analytical labs required for method development activities that lead to characterization and profiling of products. We have a young and passionate team which can be leveraged to suit the requirements.

Our Services

Over the past 10 years, PSC, has expanded its spectrum by establishing state-of-the-art Laboratories facilities and provides research & development services. Also a nexus of services such as :

Formulation Development

• Pre – formulation
• Formulation
• Lab Scale Trials
• Compatibility Studies
• Scale – up Feasibility Studies
• Stability Studies

Process Development

• Critical Quality Attributes
• In Process Controls (IPCs)
• Design Space (QbD)
• Production Validation
• Production Transferability
• Production Scale – up

Analytical Development

• Analytical Development
• Analytical Validation
• Multimedia Dissolution Studies
• Methods: HPLC, GC, Dissolution Testing USP 1 & 2
• Flow Studies
• Solubility Studies

Expert reports & Clinical studies

• Clinical expert reports
• Toxicological expert reports
• Bioequivalence studies
• Comparative clinical studies
• Clinical efficacy studies


• Documentation preparation
• Regulatory Strategy
• Regulatory services (CTD preparation etc)
• Regulatory submission & approval

Work at Pelmy Science Cyprus


Work at Pelmy Science Cyprus

On our team, everyone makes an impact. It starts from within each of us, and when we bring our expertise together, we make a significant difference—to our team, to our customers and to the world.

You’ll discover resources that match your professional development interests, a culture that welcomes your ideas and opportunities that only a leader can provide.

As part of our multinational team, what you do contributes directly to our mission: enabling our customers to make the world healthier, cleaner and safer.

Our Partners