Do You Need A WDA? Here Is What You Need To Know
There has been an increase in the number of companies that have sought our services to assist them in obtaining a WDA. If your company needs a WDA, we can assist you with the process in a timely and professional manner. This blog from our Quality team looks at the issues that you will need to consider if you need a WDA.
- Identify the scope of the Wholesale Distribution Authorisation
- Provide a Responsible Person (RP)
- Prepare & Submit the Wholesale Distribution Application to the HPRA
- Create a Quality Management System for the management of wholesale distribution activities
- Provide Quality Support to manage and maintain the Quality System
Identify the scope of the Wholesale Distribution Authorisation (WDA)
Acorn Regulatory can assist the client in identifying the category of the product authorisations that the Wholesale Distribution Authorisation will contain:
- Products that have a Marketing Authorisation in EEA country(s)
- Products that do not have a Marketing Authorisation in the EEA, but are intended for the EEA market
- Products that do not have a Marketing Authorisation in the EEA, and which are intended for export
Acorn Regulatory will also identify the type of operations required if you need a WDA:
- Procurement – Purchasing or Buying medicinal products from manufacturers or other wholesale distributors
- Holding – Physical Storage of Medicinal Products
- Supply – Providing, selling or donating medicinal products to other wholesalers, pharmacists, or persons authorised to supply medicinal products to the public
- Export – Supplying medicinal products to a country outside of the EU member states or a contracting state of the EEA
Acorn Regulatory will also assist the client in identifying the categories of medicinal products with additional requirements (as per HPRA Guide to New Applications and Variations to Wholesale Distribution Authorisations, AUT-G0152-1):
- 3.1 Products according to Art. 83 of 2001/83/EC3
- 3.1.1 Narcotic or psychotropic products
- 3.1.2 Medicinal products derived from blood
- 3.1.3 Immunological medicinal products
- 3.1.4 Radiopharmaceuticals (including radionuclide kits
- 3.2 Medicinal gases
- 3.3 Cold chain products (requiring low-temperature handling)
- 3.4 Other products
- 3.4.1 Prescription only medicinal products
- 3.4.2 Medicinal products for general sale
- 3.4.3 Over the counter medicinal products for sale through pharmacies only
- 3.4.4 Unauthorised medicinal products (medicinal products which do not hold a marketing authorisation for Ireland, but can be supplied to markets outside of Ireland where the products are authorised)
- 3.4.5 Vaccines
- 3.4.6 Parallel imported medicinal products authorised by Parallel Product Authorisation (PPA) 3.4.7 Parallel imported medicinal product authorised by Dual Pack Registration (DPR)
- 3.4.8 Parallel distributed centrally authorised medicinal products
- 3.4.9 Traditional herbal medicinal products
- 3.4.10 Homeopathic medicinal products (HOR and HOA)
- 3.4.11 Exempt medicinal products (a medicinal product which does not hold a product authorisation in Ireland but is intended for supply to the Irish market)
- 3.4.12 Biological products
- 3.4.13 Advanced therapy medicinal products
Provide a Responsible Person (RP)
Acorn Regulatory can provide the client with a Responsible Person (RP) for the Wholesale Distribution Authorisation.
The duties of the RP are:
- To oversee the procurement and supply activities
- Approve Bona Fides of new Suppliers, Customers and Service Providers
- Ensure that the activities of the Wholesale Distribution Authorisation comply with the guidelines outlined by the HPRA, and with the scope of the WDA.
Acorn Regulatory will ensure that the RP is qualified and trained for the role of the RP at the wholesaling premises.
Acorn Regulatory can also provide RP training to the client for a person identified by the client as a suitable RP.
Prepare & Submit the Wholesale Distribution Application to the HPRA
Acorn Regulatory can provide & submit the Wholesale Distribution Application to the HPRA, on behalf of the client, in the form of a submission package which comprises of the following:
- Letter of Application
- WDA Application Form comprising of signed declaration
- Certificate of Incorporation
- Statement on-premises & equipment
- Overview of documents and records
- Statement on the Quality System
- Classification of facility size
- Documents relevant to the RP
- Job Description
- Training Records
Create a Quality Management System for the management of wholesale distribution activities
Acorn Regulatory can provide the client with a complete Quality Management System, comprising of SOPs (Standard Operating Procedures), Forms, Logs/ Trackers and any other relevant process which will enable the client to perform and manage the procurement and supply activities of the WDA, whilst maintaining compliance with the requirements of the HPRA Guide to Quality System for General Sale Wholesale Distributors.
Provide Quality Support to manage and maintain the Quality System
Acorn Regulatory can provide the client with a Quality Support representative, for the purpose of managing and maintaining the Quality System associated with the Wholesale Distribution Authorisation. Activities of the Quality Support representative can include but is not limited to:
- Documentation Control
- Process System Control (Change Control, CAPA (Corrective Actions/ Preventive Actions), Risk Assessments)
- Control and Monitoring of Training
- Quality Management Review preparation
- Investigation and Management of Customer Complaints
- Assisting with Bona Fides for Supplier, Customer, and Service Provider approvals
The duties of the Quality Support representative also include ensuring that the activities conducted under the Wholesale Distribution Authorisation comply with the guidelines outlined by the HPRA and that the activities conducted are within the scope of the WDA. The Quality Support representative will also act as a supporting function for the Responsible Person and any other member of the Quality Team.
Acorn Regulatory will ensure that the Quality Support representative is qualified and trained for the role of Quality Support for the WDA.
If you would like to talk to us about your WDA requirements, please contact us on 00353 52 61 76 706 or complete the form below and we will get back to you.
We understand that not every small to medium-sized company can develop, implement, and maintain a Quality Management System (QMS).
Our team can work with your organisation to put an effective and functioning QMS in place in addition to providing the mandatory services of a Responsible Person (RP) or a Qualified Person (QP). This outsourced option or ‘contract RP’ or ‘contract QP’ is a cost-effective means of addressing the requirement for full oversight of manufacturing and supply chain activities.
Read more, here.