Need assistance complying with Saudi FDA (SFDA) medical device regulations?

Need assistance complying with Egypt EDA medical device regulations?

Alshedwy Group is a leading resource for helping you access two of the most emerging and fast-growing medical device markets worldwide. With our native and local knowledgeable teams in both Egypt and Saudi Arabia, we are ready to assist you with medical device and IVD registration, Licensing, listing, local regulatory representation, and distributor qualification.

Alshedwy commercial and industrial group of companies. aka “Alshedwy Group” has established Hatem I. Alshedwy Comm. Est. to act as the Regulatory Affairs arm regarding its business in health care sector within the Kingdom of Saudi Arabia, in response to the new regulations adopted by the Saudi Food and Drug Authority SFDA beginning from January 2012.

Alshedwy commercial and industrial group of companies. aka “Alshedwy Group” has established Alshedwy Egypt Est. to act as the Regulatory Affairs arm regarding its business in health care sector within Egypt, in response to the new regulations adopted by the Egypt Authority EDA beginning from January 2013.

Alshedwy Group, Saudi Arabia is proud to present a full range the Saudi Regulatory Affairs Consultation Services concerning Medical Devices to both local and overseas manufacturers that wish to put their MD/IVD products into the Saudi market and need to comply with the SFDA regulations.

Saudi Authorized Representative (Saudi Auth. Rep.) is the most important prerequisite for MD manufacturer to get into the Saudi market as obligated by regulations, Alshedwy Group acts as the native Saudi Auth. Rep. for many MD manufacturers and also has strong affiliation agreements with some of the esteemed global regulatory affairs consultancies.

Please contact us at your convenience for a free consultation at: +966 502015100 or regulatory@alshedwygp.com

Hatem I. Alshedwy Comm. Est.,

P.O.Box # 4596 Makkah 21955 – KSA

Alshedwy Group, Egypt is proud to present a full range the Egypt Regulatory Affairs Consultation Services concerning Medical Devices to both local and overseas manufacturers that wish to put their MD/IVD products into the Egyptian market and need to comply with the EDA regulations.

Egypt Registration Holder (ERH) is the most important prerequisite for MD manufacturer to get into the Egyptian market as obligated by regulations, Alshedwy Group acts as the native Egyptian Auth. Rep. for many MD manufacturers and also has strong affiliation agreements with some of the esteemed global regulatory affairs consultancies.

Please contact us at your convenience for a free consultation at: +20 1159113555 or egypt@alshedwygp.com

Thank you for your attention, and we are looking forward to work with you in the future!

Alshedwy Group, your Medical Device Compliance Consultants