Wholesale Distribution of Pharmaceuticals
We can provide a professional service of:
- Contract Responsible Person (RP) / Deputy RP
- Wholesale Distribution Authorisation – WDA Application
- Good Distribution Practices (GDP) Compliance
- GAP Analysis and Pre-Inspection Audits
- GDP/ RP Training
- Quality Systems – Build, maintain and the maintenance
- Risk Assessment – Development and mitigation
- Audit Planning – Delivery and Corrective Action
Flexible Training and Workshops
We can offer a wide range of courses presented by professional trainers. Our courses are filled with informative and inter-active workshop content.
Pharmacist and Pharmacies
We can help entrepreneurs gain their own pharmacy by aiding with:
- NHS Contract Application
- GPhC Registration
- Standard Operating Procedures (SOP)
- Recruitment
Is your current pharmacy business at risk? We can consult you on:
- Scoping gaps in the local pharmacy services provision?
- “SWOT” analysis, bespoke marketing plan
- Essential Services Support
- GPhC Inspection preparation
- Automation and Optimisation
- Business Development
Care Quality Commission
We can be your ‘one stop shop’ for CQC Registration and Compliance. We can help with the following:
- CQC registration
- Documentation
- Quality Management Systems
- Pre Audit Analysis
- Risk Profiling and Compliance
- Bespoke Consultancy
- Business improvement
- Training and practical implementation
Latest News
Face to face training more Benefits than you might think
You work in different ways to others, just the same as I do. However, for me (and maybe you) it just works when I learn face to face.
The General Pharmaceutical Council to Reinstate full CPD revalidation
The Government recently announced that the emergency powers that were put in place by the Secretary of State for Health and Social Care to help with the response to the COVID-19 pandemic, will be removed later this year.
Medical Devices – Consultation on the future regulation of medical devices in the United Kingdom
Following the UK’s exit from the European Union (EU), the government identified a unique opportunity to improve how medical devices and in vitro diagnostic medical devices (IVDs) are regulated in the United Kingdom.