ISO Standards

Blueberry Therapeutics sign up to ComplianceControl Centre

Blueberry Therapeutics, a modern drug discovery and development company based at Alderley Park, Cheshire have signed up to ComplianceControl Centre (CCC). Blueberry Therapeutics have extensive knowledge and experience in developing drugs from the concept stage, through regulatory approval, clinical proof of concept and beyond.

Blueberry Therapeutics’ ultimate objective is to create novel, safer and effective medicines to treat diseases in both humans and animals. Blueberry Therapeutics focuses on the research and clinical development of treatments for inflammatory and infectious diseases such as inflammatory bowel disease, atopic dermatitis, acne, fungal diseases and anti-microbial resistance (AMR).  Using its patented, safe, nanoparticle drug delivery platform, Blueberry is developing novel peptide medicines that directly target mechanisms of bacterial resistance. By doing this Blueberry can restore sensitivity of bacteria to standard antibiotics.

ComplianceControl Centre has recently launched version 3.5 of its electronic Document and Quality Management System, that will be used to cover all aspects of Blueberry Therapeutics’ Quality and Compliance Management system, including ISO 13485. The system will manage documentation, equipment, training records, audits, and corrective actions and preventative actions, to ensure proactive compliance management and will be particularly useful providing visibility of compliance across all the Blueberry Therapeutics offices and laboratories.

Dr Mike Davies, Blueberry’s Co-Founder and Chief Medical Officer, explained: “As we are now moving into the clinical phase of our business plan we needed to ensure that all our processes and data handling are compliant with current European and USA regulations. This is particularly important for our clinical trials programmes.

Blueberry is a small, agile company working across several locations and we wanted a simple, cost effective, and validated solution for a price that we could afford. The CCC “out of the box” solution allowed us to move quickly to a working system and we are very pleased with the service and support we have received from the company to date”.

Sean Forrest, Operations Manager of Compliance Control Ltd. stated: “We are pleased with the latest release of our software, which has been developed with help from the Technology Strategy Board Grant awarded in 2012 and funding from the Northwest Biomedical Fund. The new Software as a Service release really does mean that SME’s, like Blueberry Therapeutics, can now have access to Quality and Compliance software traditionally only available to larger organisations at an affordable price applicable to many small start-up and growing companies”.

Forrest continued: “Blueberry Therapeutics wanted a system that could be available and validated immediately, so that they could spend time using the system, not designing, customising and validating it. ComplianceControl Centre is an ‘Off the Shelf’ (GAMP®5 Category 3) product, which means that the system can be operational and fully validated within five days.”

ComplianceControl Centre, is a Software as a Service (SaaS) Electronic Quality and Document Management Software System that provides real-time visibility of the complete Quality, Compliance and Validation status of an organization.

Compliance Control Ltd. provide Compliance, Validation and Quality Consultancy Services and Products to the life science and pharmaceutical global markets. Services include Compliance and Validation planning and strategy, Documentation and Testing, along with a series of Auditing services and Computer System Validation Training courses.

For more information, please visit:

Compliance Control Ltd.

Winnington Hall,

Winnington, Northwich

Cheshire CW8 4DU

United Kingdom

Contact person: Sean Forrest

+44 (0) 1606 871113


Blueberry Therapeutics Ltd.

Blueberry Therapeutics is a modern drug discovery and development company with a unique nanopolymer drug delivery technology.  This opens up huge opportunity to rapidly develop new medicines, and help us find ways to treat infection and inflammation. 

For more information, please visit:

Blueberry Therapeutics Ltd.

The BioHub at Alderley Park


Alderley Park

Alderley Edge


SK10 4TG

United Kingdom 


t: +44 (0) 1625 238776


Customer References

  • I can certainly recommend Compliance Control as experts in this field and they will add value and deliver on your project. CFO, Major Pharma Company
  • Compliance Controls Consultants brought immediate expertise to our team as part of our drive into the European market. Vice President, Research & Development, Pharma Company
  • We wanted an organization with proven experience ensuring our organization can meet EU regulatory requirements. Business Development Manager, Phama Company
  • I would like to personally express my great appreciation for all your excellent work and great support with the validation of our IT infrastructure and software. Managing Director, Compounding Centre, UK
  • ComplianceControl Centre was selected because it is easy to use, quick to set up, and was a validated, cost effective solution for an organization of our size. We wanted a system that we could rapidly implement. Vice President, Research & Development, Pharma Company
  • Working with Compliance Control Consultants and their software products ComplianceControl Centre and cGARD helped us to understand the regulatory requirements of IT and business systems more clearly. IT Director, Pharma company
  • Using ComplianceControl Centre will help us to ensure that we are always inspection ready, by tracking our critical Quality and Compliance activities. Vice President, Research & Development, Pharma Company
  • It has been a pleasure working with you and your team and I am looking forward to co-operating with your company on similar projects in the future. Managing Director Compounding Centre UK
  • Based on your achievements and delivered results, we have started the process of building up our internal team for continuation of the work started by you. Managing Director, Pharma Company
  • cGARD has become the new rage here ! Sr. Manager, Documentation and Training, Major Pharma Company





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