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Regulatory Affairs & Documentation Specialist with over 15 years of experience supporting legal and regulatory functions in multinational organizations. Skilled in preparing regulatory submissions, managing product documentation, liaising with GCC authorities, and ensuring compliance with regional regulations. Adept at coordinating cross-functional teams to deliver accurate documentation under strict deadlines.
Experienced in managing large client caseloads through diligent planning and project coordination. Investigates with due care and diligence to identify concerns and achieve positive outcomes. Communicates and presents confidently to engage staff, stakeholders and clients in program activity.

A Regulatory Affairs, Business oriented professional, with extensive expertise in the pharmaceutical regulatory field.
Excellent Project Management skills, capable of delivering key communications with clarity, impact and passion.Ability to lead and offer creative solutions to regulatory problems, while balancing the expectations of Health Authorities.Ability to Recognise potential long term issues for projects..


  Training and practice in good laboratory practice which includes application and set up of basic analytical methods and synthetic reactions in an organic laboratory along with the adoption of a safe behaviour in a laboratory environment during elaboration of my undergraduate thesis project at Laboratory of Medicinal Chemistry of Department of Pharmacy, University of Patras.
  Familiarity with improvement of drug treatment (dosage assessment base on liver and/or kidney function, checking for possible drug interactions, spotting drug toxicity and adverse reactions and implementing efforts to minimize them) during my clinical practice in various private and public hospitals in Athens Metropolitan Area which constituted the whole 3rd semester of my postgraduate studies in Clinical Pharmacy and included visits with clinicians in inpatients.
  Training and familiarization with the general principles of Quality Assurance in the stages of delivery, storage and distribution of pharmaceuticals products also during my work experience in central pharmaceutical store of Hellenic Navy.


Results-driven and detail-oriented Regulatory Affairs Specialist with expertise in the medical device and pharmaceutical industry in Bahrain. Possesses a comprehensive understanding of local and international regulations, coupled with the ability to effectively manage regulatory submissions, maintain product registrations, and develop regulatory strategies. Keeps abreast of emerging trends and changes in the medical device industry, providing valuable insights and regulatory intelligence to stakeholders. Skilled in effectively communicating with regulatory authorities and responding to inquiries to ensure smooth interactions and compliance.

Lovelyn Kate Sumicad

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Regulatory Affairs Officer

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Bachelor of Science - Pharmacy

Junior High School and Senior High School - undefined

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Regulatory Affairs Officer

Junior High School and Senior High School - undefined

Bachelor of Science - Pharmacy

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