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Skills

  • Pharmaceuticals
  • Requirements Analysis
  • Biopharmaceuticals
  • Consultant
  • Marketing
  • Medical
  • Medical Device Design
  • Project Management
  • Training

Services

  • Pharmaceutical Regulatory Affairs

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    Preparing drugs regulatory files for submission to authorities in different countries according to the local requirements.

    BiopharmaceuticalsPharmaceuticalsProject Management
  • Pharmaceuticals Regulatory Affairs

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    Giving advices to marketing authorization holder to fulfill local registration requirements. Work closely with MAH to fulfill these requirements.

    MarketingPharmaceuticalsRequirements Analysis
  • Pharmaceuticals Regulatory Affairs

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    Helping in carrying out stability studies for drugs according to local climatic zones where drug will be marketed.

    Pharmaceuticals
  • Pharmaceuticals Regulatory Affairs

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    Carrying out Seminars and Lectures on different Regulatory affairs subjects and issues and the latest ICH quality guidelines.

    Pharmaceuticals
  • Medical Devices Regulatory Affairs

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    Preparing Medical Devices registration files and helping in devices classification and the best registration pathway.

    MedicalMedical Device Design
  • Pharmaceuticals Quality Control

    $5/hr Starting at $25 Ongoing

    Dedicated Resource

    We provide pharmaceuticals quality control consultancy based on ICH guidelines and local competent authorities requirements.

    ConsultantPharmaceuticalsRequirements Analysis

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About

our mission is to help our customers in obtaining marketing approvals in targeted countries and following up drugs status during the marketing approval validity.

My name is Mustafa Hamido and I am 34 years old. I have worked in pharmaceutics field since my graduation from university in 2005. I joined the regulatory affairs field in 2009 and worked in Dubai local firm for 3 years. I have followed UAE local requirements and products registration process before I decided to move to Dublin, Ireland and get a broader view on regulatory and quality subjects. I joined Trinity College of Dublin and studied Pharmaceutical Analysis master program. I was exposed to a quality, analytical and regulatory modules there. I have got a broad experience in these fields and became aware of all subjects relevant to medicines and its quality and regulatory issues. I then joined a firm specialized in personal care products and worked since then with them as quality consultant.

During my work and academic studies, I participated in obtaining importing permits for drugs and medicines and I have a little experience in it. I followed during my work experience UAE registration process for medical devices, drugs and combination products. Actually for drugs and biologicals; UAE registration process is the same of the ICH registration guidelines and modules. It follows the requirements mentioned in ICH guidelines and adopt all its requirements. Only small differences can be seen in Module 1 of the CTD structure. These differences are mainly administrative differences and not by anyway relevant to quality or safety and efficacy issues. I was exposed also to EU registration requirements and FDA registration requirements during my academic study and especially EU registration process (EMEA) adopt the ICH requirements I studied in details.

Work Terms

1- Communications are done through our mail mustafahamido@gmail.com.
once you sent a mail, we will contact you to understand your needs and put a proper plan for your cases.

2-Each request is known in our files as a case. once we reach to a deal with our customers, we will establish a case in our system and that case will have a reference number to ease following it.

3- A contract between us and customers will be signed clarifying the service type, price and all terms which will be applied.

4- 70% of the service price must be paid in advance.

5- Payment method will be through the site through paybal or direct transfer.
6- Working time is from Sunday to Friday from 6 am GMT till 5 pm GMT.