Services

Regulatory support

Nowadays, out-sourcing is a very effective solution. Many Healthcare companies whether pharmaceutical or Medical device companies are outsourcing their Regulatory Affairs function when it comes to the Middle East and Africa region. Not only does this ensure smooth operations but it can also mean less risk and less costs. MERAS can act as your dedicated […]
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Regulatory Affairs Training

MERAS organizes pharmaceutical regulatory affairs training courses, webinars and conferences as well as in-house training tailored to clients’ needs. Our courses cover pharma and medical devices. We Develop up to date content that covers the regulatory environment within the region. Our courses are designed to provide you with the required knowledge of regulatory affairs to […]
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Market Access

In MERAS, we explore and analyse market access opportunities tailored to the product, enabling our client to enter the target market in the middle east before / without registration whenever this is relevant and applicable. In addition, after understanding our customers market, MERAS studies the strengths, weaknesses, opportunities and threats that might face our client […]
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Documentation and Archiving

MEA regulatory procedures differ significantly. Responses to Health Authorities need a deep understanding of those procedures as well as HAs expectations which is one of the strengths that our experts have. Our experts have deep understanding of the regulatory documents needed by regulatory authorities in Middle East and Africa region.  MERAS applies a thorough review […]
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Labeling and Artwork

MERAS provides Arabic containing label that complies with the requirements in the Middle East and Africa (MEA) region in the shortest possible time and with best quality. MERAS provides support and guidance with packaging and labeling guidelines, artwork processes and artwork management for pharmaceutical products and medical devices that complies with the regulatory requirements in […]
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Regulatory Documents Review

MEA regulatory procedures differ significantly. Responses to Health Authorities need a deep understanding of those procedures as well as HAs expectations which is one of the strengths that our experts have. Our experts have deep understanding of the regulatory documents needed by regulatory authorities in Middle East and Africa region.  MERAS applies a thorough review […]
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Distributor Management

International Healthcare companies do face challenges in their relationship with distributors in the Middle East and Africa region. MERAS provides consulting services to companies regarding distributor performance, with some minor modifications you can ensure that you can increase revenues and profit margins.   MERAS Supports in: Creating a distributor SWOT analysis and route to market plan […]
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Regulatory Strategy

MERAS provides tailored strategic guidance to achieve the best possible outcome by evaluating the different regulatory procedures available and how they apply to your product. Getting the regulatory strategy right from the beginning is the key to ensure optimum results and bringing your products to market. Our experts besides having years of experience in the […]
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Regulatory Intelligence

MERAS provides regulatory intelligence that allows you to stay up to date with the dynamic and challenging regulatory environment in the region. We also support you in understanding the significance of key regulatory documents and their potential impact on your product portfolio. This ensures an easy flow for drug approval process and medical devices registration.
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Product Registration

A successful registration is the way to a successful marketing authorization. MERAS manages the whole registration process: Compiling dossiers Completion of country specific forms Preparation of price certificates Continuous assessment of the dossier and providing the right solution MERAS provides regulatory affairs advice as one of the regulatory affairs consulting services at all stages before […]
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