Acheiving

Remarkable

Customer Care 

We are proud to introduce ARC Pharma (UK) Ltd a GMP Certified Contract Laboratory, a new name in Pharmaceutical and Healthcare analytics, but old hands at providing our clients with an outstanding, quality driven service. ARC offers analytical laboratory testing, from advanced R&D research projects to routine quality testing. We provide these services through experienced and expert chemists, analysts, technicians and laboratory management. Ongoing investment in the best people and equipment helps us keep ahead of the game, maintaining the highest levels of reliability and service. ARC also provides materials testing services for a broad range of clients in diverse markets and industries.

Using analytical laboratory techniques, laboratory instrumentation and testing methods, we provide our clients with critical analysis information. Whether it’s research, quality control or just plain trouble-shooting, our aim is to give you the crucial support you need to help your business meet its research, development, patient safety and quality goals. 

QUALITY IS OUR POLICY 

We recognise the fact that our clients expect only the highest standards of analysis, data, compliance and confidentiality. At ARC Pharma, quality starts at the top, with effective management and is evident throughout the company in the pride our staff take in how their expertise, ability and efficiency contribute to our clients’ success. Accredited quality standards for our operations and equipment, plus highly qualified personnel are continuously improving our offer.
At the heart of our business, we ‘Believe in Quality’.

WHY CHOOSE ARC 

Could it be our commitment to build a long-term trusting relationship which provides each client with a bespoke service? It may be our ‘get it right first time’ attitude, encapsulating the efficient way we go about our business, fully understanding the brief, thoroughly testing and checking results, meeting promised deadlines and communicating clearly. And all at a fair price!

SERVICES 

QC BATCH RELEASE TESTING

We understand the importance of outsourcing this key supply-chain process. We offer QC batch release testing for finished products, intermediates, raw materials and a wide range of pharmaceutical compounds and dosage forms

TEST METHOD DEVELOPMENT

We have extensive experience in developing analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method development activity to meet your requirements. This includes project planning, protocol writing, execution, and final development reports to satisfy your regulatory needs.

TEST METHOD VALIDATION

We have extensive experience in validating analytical test methods for various applications and across a variety of product types in compliance with international regulations. We can assist throughout the entire method validation activity to meet your requirements. This includes project planning, protocol writing, execution, statistical evaluation and final validation report writing to satisfy your regulatory needs.

PHARMACOPOEIAL TESTING

We specialise in offering GMP compliant pharmaceutical testing services. We have the ability to perform a vast array of analysis on pharmaceutical finished products, raw materials and other ingredients, from a variety of compendiums.

DISSOLUTION PROFILING

Dissolution is a critical parameter of pharmaceutical dosage forms. It is well recognised that in-vitro dissolution testing is relied upon to screen formulations during development and to ensure batch-to-batch quality control during routine release testing. Dissolution is the process by which a solid solute enters into solution in the presence of solvent. Dissolution rate may be defined as the amount of active ingredient in a solid dosage form dissolved in unit time under standardised conditions of liquid/solid interface, temperature and media composition.

TECHNICAL PROJECTS

Arc has extensive analytical testing and technical support services to assist pharmaceutical and healthcare clients achieve their regulatory registration goals and technical troubleshooting. We always solve problems quickly and accurately, backed up by clear communication with clients.

cGMP LABORATORY FACILITIES

We have an advanced range of equipment for analytical and physical chemistry analysis to support both technical projects and routine GMP compliant QC testing. We recognise that the quality and capability of our laboratory facilities is of great importance. This is why we put continuous investment into our world-class facilities to ensure we deliver exceptional value to all our clients.
We can accommodate all work requests from standard routine QC testing to more complex analytical problem solving. Combined with our state-of-the-art facilities we also enjoy building strong working relationships with analytical equipment suppliers, contract facilities and University research departments to offer you complete laboratory services within one facility.

GxP AUDITING & CONSULTANCY

We also provide GxP auditing & consultancy services as per national and international regulations i.e. ICH (Q7, Q10 etc.), EU GMP, US FDA (21CFR 211 & 210) or any other market specific regulations.

Different types of auditing and consultancy services we provides are GMP/GDP Quality audits of different types of manufacturers i.e. API & intermediates/excipients, Finished products, Distributors, Contract testing laboratories, Packing materials within EU & Asian countries on behalf of clients. We also perform GPvP/GCP Audits, ISO 13485 Audits (medical device), pre and post-inspection audits.

Arc has the excellent team of Certified (IRCA/CQI/ASQ-CQA/ISO) Lead Auditors and consultants from internationally identified auditing bodies. Our auditors are fully qualified and highly experienced in auditing and consulting in multinational pharmaceutical/chemical companies worldwide. Audit reports generated by our auditors are fully compliant and acceptable to regulatory authorities, Qualified Persons and other contract givers of different countries and regions worldwide.

NEW STANDARDS 

We are proud to introduce our exclusive UK Distribution for Pharmaffiliates Standards. We have access to over 7500 standards which are available in ready stock. Each working standard is provided with its Certificate of Analysis, Chromatographic purity, infra-red spectra, NMR and MASS spectra with its interpretation.

Pharmaffiliates have been producing standards for over 14 Years and have been accredited with ISO 9001-2008, ISO 17025 and US FDA. They are India’s largest suppliers for Synthetics.