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HomeRegulatory affairs - Sulinda

Regulatory
affairs

Regulatory surroundings are compelling and complex nowadays that licensing applications for products in the Saudi food and drug government agency sometimes fail to receive approval from the first time and takes a lot of time.

Companies are required to have essential knowledge and requirements of all Saudi FDA regulations before proceeding for their business expansion in Saudi Arabia.

The probability cost of these failures is in millions. This is why we’re here to help and guide you over the difficulty and complex process of registering a product in the Saudi FDA.

SuLinda has its own Regulatory Affairs department to offer regulatory support for Pharmaceutical and healthcare company’s field. We offer regulatory submission services related to Food, Cosmetics, herbal, medical Devices and drug Products in Pharmaceutical Companies.
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Value added service?

We provide precise Regulatory strategies and highest quality submissions to agencies globally.
Healthcare companies face challenges like knowing Saudi FDA requirements and new guidelines.
SuLinda Regulatory team can meet any regulatory requirement of companies across Saudi Arabia.
Our team follows the best ethical practices, for organizing regulatory registration steps.
SuLinda Company assures that healthcare companies should be aware of the Saudi regulations and also of any regulatory guideline.
It then becomes important that regulatory perceptions address all these challenges that the healthcare companies face precisely.

What's Included?

Products categorization and classification
Opening account in Saudi FDA systems
Manufacturing Sites Registration in Saudi FDA
Products variation and certificates renewals
Submission files reviewing
Products Submission
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