In December 2017, we celebrated our 7th Anniversary here at Clarity Compliance Solutions. To celebrate we are delighted to have launched our brand new website. Why not take a look around and let us know what you think, you could be in with a chance of winning a bottle of champagne.

Have a drink on us

Our new website - to better reflect our services and products we have launched our new website, please feel free to take a look around, let us know your thoughts and get in touch feel we could be of any assistance.

Your chance to win a bottle of champagne - to celebrate our 7th Anniversary and as a thank you for your feedback, we are giving away a bottle of champagne.  To be in with a chance to win all you need to do is, click the link here, and send us your comments about our new website.

A winner will be picked at random and we will inform the lucky winner after 9th February 2018.

We have come a long way in 7 years, having worked tirelessly in developing our range of services and products, expanding our extensive network of highly skilled and knowledgeable professionals, whilst supporting clients within the Pharmaceutical, Biotech, R&D, Bloods, Medical Devices and to their suppliers of equipment and computerised systems.

Leading the way in Data Integrity

We could arguably be described as leading the way in the industries hot topic of Data Integrity. 

David Thompson, Managing Director and Principal Consultant of Clarity Compliance Solutions, will be a guest speaker at the First International Conference on Data Integrity in Pharmaceuticals.

Due to be held on 2nd March 2018, at PriceWaterhouseCoopers, 1 Embankment Place London WC2N 6RH, David will join eleven of the most knowledgeable experts in the industry, from current MHRA and former EMA and FDA officials.

You can find out more and register for the conference here.

The MHRA and FDA Data Integrity guidelines have raised many questions for the industry on the whole aspect of Data Integrity and Computer Systems Validation. Our specialist personnel and project delivery teams have worked with small, medium and large organisations delivering Data Integrity and Computer System Validation Program support.

Our approach includes:

Data Integrity Auditing - understand your DI exposure

• DI Site Audit (benchmarking and assessment)
• DI Program Audit (on going DI program vs best practice)

Data Integrity Training - ensuring competency of your team

• DI for Management (half day)
• DI for Practitioners (full or one day)
• DI for Operational Staff (full day)

DI for Staff - (short online course for training the masses)

Data Integrity Toolkit - leverage and tailor our tools

• DI Policy, DI Strategic Plan & DI Project Definition
• DI Assessment Checklist & Procedure
• DI Implementing Positive Quality Culture
• DI Standard Operating Procedure (SOP) Review
• DI Risk Management Tools
• DI Reporting Tools
• DI into New Project Development Lifecycle
• DI Project Handover Criteria

What our customers are saying about us

We have received superb feedback from our clients:

“I would strongly recommend Clarity Compliance Solutions for all aspects of Data Integrity.

Clarity have set up and led our Data Integrity program, delivering excellent training to our management and program teams, setting up our DI governance systems and weaving DI into the fabric of our organisation, project managing and leading our assessments, setting up our risk assessment and remediation processes.

All of this done in a very professional effective and efficient manner. Throughout the program we have leveraged Clarity's experience on DI and the wider CSV and Quality Systems compliance areas and we are a much richer organisation for this.

We have recently been audited by a number of clients who have stated "... you are well ahead of where we are on our Data Integrity compliance program...".

Clarity's support and drive has taken a huge weight off my shoulders.

I am delighted with how Clarity Compliance Solutions have helped us and once again would strongly recommend them for Data Integrity, CSV and Quality Systems compliance."

Helen B, Quality Director, Contract Manufacturer

You can find out more about our Data Integrity services here.

Our Integrated Approach

In addition, to our Data Integrity and Computer Systems Validation (CSV) services, we continue to provide expertise in Business Systems Validation (BSV), Manufacturing Enterprise Systems (MES) and Laboratory Information Management Systems (LIMS), Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).

Through our strategic governance and advisory services, fused with our comprehensive training delivery and auditing services we continue to meet the needs and requirements of our clients.  Enabling them to focus their efforts and energy on day to day business, instead of losing sleep over compliance and spiralling costs.

'A one stop shop for your compliance needs - we provide full lifecycle consultancy for key compliance areas'.

Online Training - with our training partner, we are delighted to now offer a suite of online training courses, which include:

• Online Data Integrity Training
• Online Good Manufacturing Practice (GMP) Training
• Online Good Distribution Practice (GDP) Training
• Online Pharma Quality Management Systems module
• Online QP Quality Management Systems Module

Taking time to learn is easy, with online training - you simply login and start learning, wherever and whenever you like. Helping you keep up to date with current regulations, guidance and regulatory expectations.

Find out more about our online training here.

Electronic Document Management Systems - the regulatory authorities are now looking for companies and organisations to be implementing Electronic Document Management Systems (EDMS).

In response, we have proactively sort out and partnered up with a leading provider of electronic document management systems (EDMS) to the life science sector.

David Thompson, Managing Director and Principal Consultant at Clarity Compliance Solutions, said:

“We work with a number of innovative life science organisations and many of them rely upon paper-based systems to manage their quality processes. For smaller organisations, this method, although limiting and often requiring excessive manual administration, can more than capably and compliantly manage an array of business processes. Yet, as these businesses grow or become more complex, the need to bolster quality management with technology increases.

After reviewing the market, we feel confident that the combination of feature-rich, user-friendly technology and direct life science design and experience makes the perfect fit for our business and our customers."

Find out more about or EDMS products and services here.

Have a drink on us

Our new website - to better reflect our services and products we have launched our new website, please feel free to take a look around, let us know your thoughts and get in touch if you feel we could be of any assistance.

Your chance to win a bottle of champagne - to celebrate our 7th Anniversary and as a thank you for your feedback, we are giving away a bottle of champagne.  To be in with a chance to win all you need to do is, click the link here, and send us your comments about our new website.

A winner will be picked at random and we will inform the lucky winner after 9th February 2018.

Thank you and good luck!