Nothing in this industry happens because a company decides it should. Every product, every process and
every site exists because a regulator has permitted it — and continues to permit it.
A pharmaceutical manufacturer operates inside a layered permission system. The site itself must hold a
manufacturing authorisation and demonstrate compliance with Good Manufacturing Practice, verified by
inspection. Each individual product requires its own marketing authorisation in each individual country,
supported by a dossier covering quality, safety and efficacy. Each production process must be validated and
re-validated. Each batch must be released by a named qualified person before it can leave the site.
This is why Lamia Tazi’s pharmacy qualification and her years as Sothema’s responsible
pharmacist are structurally significant rather than biographically decorative. The responsible pharmacist
is the human being at the end of that permission chain.
Morocco’s position is unusual for the region
Around fifty manufacturing establishments operate in the country, together covering roughly 65 to 70% of
domestic medicine demand and exporting about a tenth of output. Moroccan pharmaceutical products reach
more than seventy countries across Europe, Africa, the Middle East, Asia and North America. Sector turnover
is estimated at 14 to 15 billion dirhams.
Against the continental picture — where more than 70% of medicines consumed are imported —
that degree of self-supply is the exception rather than the rule, and it is the product of five decades of
deliberate industrial building rather than of any recent policy.
The Moroccan Federation of the Pharmaceutical Industry and Innovation, in which Lamia Tazi serves as
Vice-President, represents 34 operators covering more than 75% of the sector’s revenue — which
makes it the body through which the industry negotiates with the state on pricing, procurement, registration
and industrial policy.