Formed in 2009, Creatifbox is a specialist design agency dedicated to the creation of market-ready artwork and creative visual solutions for the pharmaceuticals industry.
Our 10 years experience in this field has seen us continue to successfully work with major pharmaceutical organisations, as a valued partner, assisting on the route to market and creation of supporting literature.
What we do
Creatifbox provides full artwork support for a product’s route to market from QRD to submission to print-ready files for manufacturing sites.
- continually keep updated on the MHRA’s latest Labelling Requirements, Best Practice and current Safety Features Legislation, this allows us to more rapidly create compliant artwork.
- work with a number of products for market in the EU and have extensive knowledge of foreign regulatory requirements, notably Scandinavia
- update existing artwork to meet new RA requirements which may, for example, include tamper evident labels or an updated design
- provide creative services – new livery design and concept for branded and OTC products
- create illustrations and diagrams based on rough drafts found on QRD/SmPC’s supplied to us. If required, we can turn these into reader friendly visuals that are ready for print.
Our process
From client QRD data we apply die-cuts, resize and then insert the correct information required for successful submission.
- Braille: Implementation of braille, it’s positioning, size and placement of the number indicator, in all EU languages.
- TE labeling: Current legislation requires the implementation of Tamper Evident Labeling, again have hands on experience on how this works with various package styles and how it impacts the information around it.
- Unique Identifier: Placement and creation of 2D data matrix code and human readable information (leatus codes, batch/EXP, medis codes) and relevant varnish free areas. We can also provide all formats of barcode.
- First draft: Copy and technical checks are carried out before pdfs are sent to the client for submission or amendment.
Patient information leaflets:
Based on manufacturing site’s sizing information we prepare the required template. At this point we can test if the proposed text will fit at required minimum 9pts. Supplied word format text is then directly placed into the prepared template and formatted for print and, if required, items such as diagrams or pharma codes are added. A first draft TVT readable pdf is then supplied for checking by client.
Post approval :
After client revisions, variations and finally approval we can then prepare, if required, artwork for print at manufacturing site. We supply original vector artwork (pdf, .ai or eps files), fonts are outlined so the artwork cannot be accidentally changed. We work closely with manufacturing sites and understand their language and varying requirements.
Contact us
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