| Name of consultation |
|
Originator |
|
December 2010 |
|
|
|
| Medicines legislation consolidation and review project |
|
Medicines and Healthcare products Regulatory Agency |
|
| ARM 69 Nicorette 15mg Inhalator |
|
Medicines and Healthcare products Regulatory Agency |
|
| Arm 71 Radian B Ibuprofen 5%w/w gel 100g |
|
Medicines and Healthcare products Regulatory Agency |
|
| Expanding the list of "never events": Policy proposals for engagement |
|
Department of Health |
|
November 2010 |
|
|
|
| Informal consultation on the provisions for patient group directions and other matters |
|
Medicines and Healthcare products Regulatory Agency |
|
| Review of medicines legislation: Informal consultation on the Medicines Act 1968 exemptions for sale, supply and administration of medicines. |
|
Medicines and Healthcare products Regulatory Agency |
|
| Consultation on draft guidance on advertising homeopathic medicines |
|
Medicines and Healthcare products Regulatory Agency |
|
October 2010 |
|
|
|
|
Equity and Excellence: Liberating the NHS |
|
Department of Health |
|
September 2010 |
|
|
|
| Consultation on the Fitness to Practise Adjudication for health professionals: Assessing different mechanisms for delivery |
|
Department of Health |
|
| Consultation MLX 370 – Intention to amend EEA Regulations 2008 |
|
Medicines and Healthcare products Regulatory Agency |
|
| Public consultation on the Veterinary Medicines Regulations 2010 |
|
Veterinary Medicines Directorate |
|
August 2010 |
|
|
|
| Phase 2 proposals to amend the ABPI Code of Practice for the Pharmaceutical Industry |
|
Prescription Medicines Code of Practice Authority |
|
Proposals to amend the ABPI Code of Practice for the
Pharmaceutical Industry 2008 |
|
Prescription Medicines Code of Practice Authority |
|
July 2010 |
|
|
|
| NCAS contribution to revalidation |
|
National Clinical Assessment Service |
|
Public consultation on continuing need for a controlled
activity category in the vetting and barring scheme |
|
Department for Children, Schools and Families |
|
Your choice of GP practice: a consultation on how to enable
people to register with the GP practice of their choice |
|
Department of Health |
|
June 2010 |
|
|
|
| Review of access to the NHS by foreign nationals RPSGB response |
|
Department of Health |
|
Arm 67 – Request to reclassify Regaine for Men Extra Strength
Scalp Solution 5% w/v Cutaneous Solution from P to GSL |
|
Medicines and Healthcare products Regulatory Agency |
|
| Fitness to practise audit report (February 2010) |
|
Council for Healthcare Regulatory Excellence |
|
May 2010 |
|
|
|
Response from the RPSGB National Pharmacy Boards to
the Consultation on the revised draft standards for the
General Pharmaceutical Council |
|
General Pharmaceutical Council |
|
A response from the Royal Pharmaceutical Society of Great
Britain to the consultation on the duty of co-operation regulations |
|
Department of Health |
|
Consultation on the revised draft standards for the
General Pharmaceutical Council |
|
General Pharmaceutical Council |
|
April 2010 |
|
|
|
| Consultation on the revised performance review process and standards |
|
Council for Healthcare Regulatory Excellence |
|
Public consultation (MLX 364): The regulation of nicotine containing
products (NCPs) |
|
Medicines and Healthcare products Regulatory Agency |
|
| Arm 68 Ibuleve Speed Relief Max Strength Gel 10% w/w |
|
Medicines and Healthcare products Regulatory Agency |
|
Arm 66 – Extended Maximum Treatment Period and Pack Size Changes
to a Pharmacy Medicine |
|
Medicines and Healthcare products Regulatory Agency |
|
March 2010 |
|
|
|
Arm 65 – Request to Reclassify Algopain - Eze 140mg
medicated plaster from POM to P |
|
Medicines and Healthcare products Regulatory Agency |
|
Consultation on measures to strengthen the medicines supply chain and
reduce the risk from counterfeit medicines |
|
Medicines and Healthcare products Regulatory Agency |
|
Consultation on the proposals to implement 'Generic Substitution'
in primary care further to the Pharmaceutical Price Regulation Scheme (PPRS)
|
|
Department of Health |
|
February 2010 |
|
|
|
MLX 366: Intention to amend the medicines for human use
(prescribing by EEA practitioners) regulations 2008 (SI 2008/1692) |
|
Medicines and Healthcare products Regulatory Agency |
|
Pharmacy in England: building on strengths – delivering the future
Draft regulations under the Health Act 2009: Pharmaceutical Needs
Assessments RPSGB response |
|
Department of Health |
|
