Dr. Pan Ei Phyu Email & Phone Number

- Maintaining and improving affiliate Quality Management System (QMS) by developing annual Quality Handbook and Quality Plan to enhance quality standards and efficiency of the company.- Has oversight of the affiliate quality risk minimization activities.- Able to organize formal management reviews which are conducted and documented and that senior management is pro-actively alerted of systemic compliance and quality issues/risks and opportunities for training or process improvement.- Compiled quarterly reports for affiliate Management Review, including collection, compilation, reporting, and analyzing relevant data.- Actively identified deviation and oversighted CPAP process to complete within the deadline for self-identified deviation and audit finding deviation.- Organized and proactively participated in inspection readiness meeting to be 24/7 ready for the audit.

- Maintain and Improve MI atlas system for handling medical inquiries by coordinating between regional MI team and affiliate team members to provide administrative and technical management support to MI atlas- Had an experience in Market Research Program(MRP) & Patient Support Program(PSP) procedures implementation for oncology and Specialty products- Act as MRP & PSP point of contact within the Affiliate to collate and provide data in the event of audit or regulatory authority inspections. (participated in 2017 DKSH MAP PV audit and no critical finding detected during audit)

-Develop medical strategy and medical plan of assigned product (Rocephin, Rocaltrol, and Bonviva) in alignment with brand strategy.-Support business objectives based on scientific evidence and clinical/medical knowledge in the specific disease area.-Execution of medical plan in proper alignment with commercial team-Provide medical input to be incorporated into product strategy and development-Perform, plan and oversight scientific communication activities with Therapeutic Area Experts (TAE)-Build and maintain long-term strategic partnership with TAE for assigned therapeutic area-Provide updated scientific information and input to all relevant stakeholders whenever required-Establish TAE profiling and mapping for strategic products in collaboration with marketing team-Perform timely responses to medical information inquiry through MI atlas system-Conduct disease and therapeutic area training and other medical affairs relevant training to new comers from the commercial and medical team.-Ensure all the scientific information mentioned in the promotional and non-promotional materials including presentation slides are scientifically robust and compliant in accordance with local SOP and global directives-Ensure all the relevant activities are compliant with symphony and healthcare compliance directives-Extend close collaboration with local safety unit and regulatory affairs for pharmacovigilance and safety communication matters.

Yangon, Myanmar

Organized and had robust experience in all medical activities including International congress (ISPD), preceptorship for Renal anemia, clinical meeting, local symposium with foreign speaker and guideline development and advisory board meeting for Rheumatoid Arthritis.Provided medical expertise to HCP and collect HCP insights and disseminate to internal product team.

In Roche, I was Product Specialist for Rocephin, Dormicum, Lexotan, Rivotril.

Yangon, Myanmar

In Sanofi, I was Medical Sale Representative for Princi B Fort, Xatral, Clexane.