Less time ticking boxes.
More hours on the ward.
MediRegs will save you time on administrative duties to help you comply with the Lord Carter Review recommendations without extra staff or overtime. Enter your email below to see how it works.
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The review recommends that trusts ensure more time spent on clinical pharmacy services. To do this means reducing other activities, such as supply chain. MediRegs helps pharmaceutical organisations comply with GDP guidelines 2013/C 343/01 (Bona Fides) without the headaches. Leaving you to focus on clinical services.
The fastest and easiest way to manage your regulatory responsibilities.
LESS TIME MANAGING SUPPLY CHAIN REGULATORY REQUIREMENTS
Know instantly if any supplier has their pharmaceutical authorisations changed by the MHRA or GPhC. Reduce the risk of breaching your regulatory responsibilities by validating which organisations have the appropriate authority to trade in pharmaceuticals.
Verify your suppliers’ authorisations – both current and historical. Check multiple sites and every license type for any organisation – not just their head office.
AUTOMATE PROCESSES AND REDUCE POSSIBILITY FOR HUMAN ERROR
Automate your current manual processes to reduce the chance of human error. Utilise staff resources more efficiently by quickly verifying your supply chain in just a few clicks.
Grant full, or ‘read-only’ access to any of your GDP or sales team staff. Record the audit trail to show which team members updated what and when.
EASILY VERIFY YOUR SUPPLY CHAIN AND COMPILE REPORTS
See the changes approved by the Licensing Authority during a specified time period for Wholesale Dealers and Active Substance Manufacturers, as well as importers and Distributors, and the types of product(s) or activities that are handled at the sites.
Keep track of your License Holder information and the type of products or activities that are approved by the regulator for each of your sites. You can also report where your licenses are cited on a Wholesale Dealers License and the type(s) or products or activities that are handled under that License.
Automate your current manual processes
Utilise staff resources more efficiently
Verify your customers’ and suppliers’ authorisations
Reduce the risk of breaching your regulatory responsibilities
MediRegs helps you to:
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Spend more time on clinical pharmacy services than supply chain activities
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Ensure office functions become more efficient to maximise value and outcomes
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Know if any supplier or customer has their pharmaceutical authorisations changed
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Check multiple sites and every license type for any organisation
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Keep track of your License Holder information
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See the changes approved by the Licensing Authority during a specified time period
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Manage your business from anywhere, with a fully mobile responsive application developed for desktop, iOS & Android
Pricing (Limited Launch Offer)
Get a Pro Account for the same price as the Regular account for the lifetime of your subscription.
Manage Your Supply Chain
Manual Verification Reports
Single User
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Manage Your Supply Chain
Automatic Verification Reports
Single User
Automatic License Alerts
GPhC Data for Pharmacy Premises
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Manage Your Supply Chain
Automatic Verification Reports
Multiple Users
Automatic License Alerts
GPhC Data for Pharmacy Premises
Sub-User Management
+ User Activity Tracking
Historical Report Archive
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Contact us for Enterprise Pricing:
Unlimited Users, Bespoke Onboarding & Custom Domain Name.
A secure solution developed by a company with a track record of solving problems in the Health sector
Common questions about MediRegs
Contact product.info@mediregs.south.co.uk if you have any questions and we’ll do our best to answer
Bronze £ 79 pcm
Silver £169 pcm
Gold £259 pcm[/foundry_toggles_content][foundry_toggles_content title=”How much does Bespoke onboarding cost?”]We recognise that many companies have their EUFMD data stored in legacy formats across multiple locations. Sometimes this might be internal databases, excel documents, or even hardcopy spreadsheets updated by hand, then duplicated and distributed. Getting all this complex information into a new format can be a lengthy and time-consuming process – especially if there are thousands of records.
We offer a bespoke onboarding service that can take all your EUFMD data and upload it into your MediRegs account. The cost for this service depend on the amount of data, the complexity and the formats involved. Please contact us for a quote.[/foundry_toggles_content][foundry_toggles_content title=”Where is the data stored?”]The site is hosted in one of two UK data centres located on the Manchester Technopark on the periphery of Manchester City Centre. The data centre facilities are totally secure, fully air conditioned with redundant power supplies and are fully supported 24/7 by an on-site Network Operations Team.[/foundry_toggles_content][foundry_toggles_content title=”Is my data safe?”]MediRegs is developed by South˚. We are registered with the Information Commissioner. We have notified the ICO and our data protection number is Z2907170. All data connections are across SSL using a 256bit key from Comodo with an AES 256bit encryption algorithm. We backup to a secure offsite location using R1Soft, which offers continuous data protection only backing up what has changed – but results in full restore points at any one time. Backups are taken daily at 9AM and 10 of these are retained, with 8 weekly archives – so we have backups every day for 10 days ago and 8 weeks worth of backups available.[/foundry_toggles_content][/foundry_toggles]