Twenty statements on one carton
The order of 14 February 2021 lists the statements for the carton, the primary packaging and the leaflet of imported medicines. Space runs out quickly.
Pharmaceutical packaging · Algiers
A medicine carton carries more than twenty statements, in Arabic and a foreign language, on a few centimetres. We design your cartons, leaflets and labels so that everything is accurate, readable and consistent from one strength to the next, based on the texts validated by your responsible pharmacist.
The real problem
In pharmacy, packaging isn’t just a shop window: it informs, identifies and protects the patient. A misplaced statement or a confused strength costs more than a reprint.
The order of 14 February 2021 lists the statements for the carton, the primary packaging and the leaflet of imported medicines. Space runs out quickly.
Statements appear in Arabic and in a foreign language used in Algeria. Any difference between the two versions is an error.
Two strengths that look too alike get confused at the counter. Colours, hierarchy and codes distinguish each product.
ANPP notes provide for statements to be brought into compliance at registration renewals and variations. Better to have a system ready to evolve.
What you get
A grid shared across the range: every new strength or update is done without rebuilding everything.
Panels organised for mandatory statements, INN and strength prominent, barcode and batch area in their place.
Bilingual layout of a long text, folding adapted to the carton, readability maintained down to the last section.
Bottles, tubes, blisters: the essentials on a small surface, without losing identification.
Colour codes and hierarchy by form and strength, so that no product looks like another.
Packaging and labels adapted to their own statements and their sales channel.
Print-ready files for the printer, tracked versions, proof reviewed with your team before every run.
How it works
The regulatory content comes from your team; we turn it into accurate, readable and consistent packaging.
The products, forms and strengths, existing packaging, the registration decision and the validated texts.
You approve: the scopeShared grid, bilingual hierarchy, colour codes by strength or form.
You approve: the range systemCartons, leaflets and primary packs laid out from the texts provided, statement by statement.
You approve: each documentCross-review with your responsible pharmacist, proof checked before printing.
You approve: the final proofFiles handed to the printer, versions archived, updates made easier at the next renewal.
You receive: packaging ready for production2-minute brief
Frequently asked questions
For imported medicines, article 13 of the order of 14 February 2021 (Official Journal no. 15 of 2 March 2021) lists them: brand name, INN, form, strength and contents, excipients with known effect, warnings, storage conditions, marketing authorisation holder and manufacturer, registration number, batch, manufacturing and expiry dates, barcode identifier, among others. For local production, they follow from your registration decision and ANPP notes.
In Arabic and in a foreign language used in Algeria, in visible, easily readable and indelible characters. Both versions must carry the same information.
Article 14 of the same order lists, among others, indications, dosage, contraindications, interactions, side effects, what to do in case of overdose, storage conditions and the text’s revision date. We turn it into a readable bilingual layout, folded for the carton.
No: the regulatory content is the responsibility of your responsible pharmacist and your registration decision. Our role is to lay it out accurately, readably and consistently, and to flag any inconsistency spotted during review.
They have their own statements (article 18 of the order for imported products), depending on their category: designation, approval number, sterilisation method, batch or serial number, certification body, among others.
Yes. We start from your current packaging, build a shared grid and update the products at the pace of your renewals and registration variations.
Yes. We can sign a non-disclosure agreement before any detailed discussion about your products.
First scoping
A few details are enough for a useful first conversation. Reply within 2 working days.
Go further
The general rules of packaging and printing, explained step by step. The guides are written in French.