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Welcome to Gizew Medicine & Medical Supply Whole Sale

About Us

Gizew Medicine & Medical Supply Whole Sale Was established in December 2014 in Hawassa, Ethiopia. The Company started its Business activities with an initial capital of 20 thousand USD with 5 Employees. Currently the Company is operating with a paid up capital of 1.2 Million USD and with more than 30 permanent employees. We believe in our qualified staff and our commitment to benefit our customers; that is what builds our company. We are working in the Pharmaceuticals Import and Wholesale, Targeting the public as well as the private health sector of Ethiopia. Our annual sale is more than 8 Million USD on the year 2022.It is increased the annual sales by 30% on the year 2023. A reliable business strategy and implementation frameworks are in place to materialize this Vision in the shortest time possible.

After Operating as a distributer company for quite some time and gaining tremendous experience in the market we decide to boost our activity by importing our own products. For this, after a meticulous planning and thorough analysis of the market we establish our own Import and Distribution Company, Gizew Pharmaceuticals Medicine and Medical equipment Import PLC.

Gizew Pharmaceuticals Medicine and Medical equipment Import PLC is a Pharmaceuticals company established in the year April 2020 G.C with a registered capital of ETB 6,000,000.00 . The company founders were motivated by a family business. The Main Business Activity of the company includes Import and distribution of safe quality Medicines, Medical Supplies and Medical Equipment’s from Henso Medical (Hangzhou) Co.LTD & Wondfo Biotech Co.LTD, China. The company also represents Tekia zeari Plastic Factory, Ethiopia for the Supply of Urine Cup, Stool Cup and Sputum Cup. The Company also represents Kilitch Estro Biotech PLC, Ethiopia for the supply of Different Medicine and Medical Supplies.

In terms of Human Resource, the company has more than 30 employees with diverse expertise including; Pharmacist, biomedical engineers, Sales & Marketing Professionals, regulatory experts backed by strong finance and administration personnel with a long-term experience in the sector.

Mission

Our mission is “Being Commited Company to respond customer needs and overall satisfaction through supplying and distributing quality, Safety and standardized Medicines, Laboratory reagents, Chemicals, Medical Equipment and providing efficient services with affordable price for our customer”.

corevalues

Our Company Core Valuess

Commitment towards its clients

Commitment towards its Staff

Commitment to quality supply

Providing a client focused marketing and claims service

A dynamism of management in reacting to fast-changing market conditions

Providing efficient claims and client service

Transparency

Accountability

Respecting the law

Call us anytime for any enquiry

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cta

Our Services

medicine

Medicine

We provide many types of medicines that have passed all inspections and are checked for their shelf life routinley.

medical-device

Medical Device

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reagent

Laboratory Reagent

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equipments

Medical Equipments

Find the quality wholesale supplies and equipment you need for your high-performing lab, physician practice or post-acute care setting. Satisfaction guaranteed.

sanitary

Sanitary Materials

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Frequently Asked Questions

Let us give you some insight into the most asked questions regarding our business and related parts.

Premarket notification, also known as 510(k) notification is mandatory registration for manufacturers to notify FDA (Food and Drug Administration) about their intent to market a medical device.

Medical devices can be classified based on required level of control to ensure safety and effectiveness of the device. As this is risk-based classification, the major class determination factor is the risk the device poses to the patient or the user.

According to FDA, Medical devices can be classified into three classes: Class I (General controls), Class II (General controls with special controls) and Class III (General controls, Special Controls and premarket approval) devices.

Design controls is a formal methodology to drive medical product development activities, which are often mandatory. Medical device manufacturers must follow design control requirements under 21 CFR Part 820.30 to market all class 2 and 3 devices as well as certain class 1 devices such as software controlled devices.

Design control is a set of quality practices and procedures that control the design process to assure that the device meets the user needs, intended uses and specified requirements as well as improve and prevent future issues.

On the highest level, design controls requires Medical device design & development planning, design input, design output, design review, design transfer, design changes and design history file.

Medical device users look for effectiveness and safety of devices that they use to address a particular problem or condition, which are sometimes critical to life. This is why iterative testing with verification and validation of these medical devices becomes imperative.

Verification and validation of medical devices in the design process aim to ensure that the device is aligned with the need of targeted users and delivers the intended solution. It also helps ensure whether all the requirements are being satisfied. It helps to comply with regulations as well as designing the highest quality product.

Standardized verification and validation activities can also streamline the manufacturing process as well as enhance approval process.
 

Contact Us

Get in touch

Location:

Hawassa, around mobile, Infront of Abera langano Furniture,

Email:

info@gizew.com

Call:

+251 913066471 or +251 910525153

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