
Closed
Posted
Paid on delivery
I need assistance with the submission of medical device applications in Thailand. The primary focus is on ensuring successful communication with regulatory authorities. Although my main requirement is communication, I am open to considering additional services such as regulatory strategy development and preparation of technical documentation for future needs. Key Requirements: - Submission of medical device applications in Thailand. - Effective communication with regulatory authorities. Ideal Skills and Experience: - Experience in regulatory affairs within the medical device sector. - Strong communication skills with regulatory bodies. - Knowledge of Thailand's regulatory environment for medical devices.
Project ID: 39696762
14 proposals
Remote project
Active 9 mos ago
Set your budget and timeframe
Get paid for your work
Outline your proposal
It's free to sign up and bid on jobs
14 freelancers are bidding on average $544 USD for this job

Hi, I can do it in the NEXT FEW HOURS by working on it right now. I would like to help you at a LOW PRICE, HIGH-QUALITY work delivered before TIME. Message me for detailed discussion. Thanks and Looking forward:). I guarantee 100% satisfaction of my clients and provide Turnitin plagiarism reports. Please see my profile and reviews from my previous clients. https://www.freelancer.com/u/DevBenchHQ Thank you
$250 USD in 1 day
4.6
4.6

Hello Sandrine, I can assist you with the submission of medical device applications in Thailand, ensuring effective communication with regulatory authorities throughout the process. I am an expert with 6 years of experience in regulatory affairs, specifically within the medical device sector. My background includes successfully navigating the complexities of regulatory environments, crafting technical documentation, and developing strategies tailored to meet specific compliance needs. My strong communication skills enable me to engage effectively with regulatory bodies, ensuring that your applications are not only submitted timely but also meet all necessary requirements. I believe my experience aligns perfectly with your project needs, making me the best fit for ensuring your success in this endeavor. Thanks, Billy Bryan
$250 USD in 6 days
0.0
0.0

Moreover, even though I don't have specific knowledge of Thailand's regulatory environment for medical devices, my fluency in different programming languages - including Go and Node.js - demonstrates my adaptability and ability to pick up new concepts quickly. This means that I'll be able to meet any additional needs you might have, such as regulatory strategy development and technical documentation. Combining this with my commitment to delivering high-quality work on time and on budget, I am confident that I am the right fit for your project. By choosing me, you're not just hiring another freelancer; you're gaining a dedicated partner who understands the value of good communication. I look forward to building a strong relationship with you and ensuring a successful submission process for your medical device applications in Thailand. Let's embark on this project together and i guarantee our collective effort will dentify us as one of the leading manufacturer in the country
$500 USD in 7 days
1.7
1.7

Hello, As a seasoned professional with 12+ years of experience, I have honed my skills in various enterprise-level business domains, and medical device regulatory affairs is one of them. With an excellent track record in project management, I thoroughly understand the importance of effective communication and adhering to regulatory standards. Thailand's regulatory environment for medical devices is something I'm intimately familiar with, providing an added advantage to navigate the complexities involved in your project. Having worked extensively with Node.js, Python, and JavaScript (including Vanilla JS), you can count on me to create efficient and robust solutions for your medical device application submissions. Additionally, my knowledge and experience in Data Science (AI & ML) can be highly valuable for regulatory strategy development and technical documentation preparation for your future needs. I promise a result-oriented approach throughout our collaboration while maintaining regular availability and adhering to project timelines - even across different time zones. My experience with various project management tools further streamlines our communication and keeps us well-coordinated throughout the process. In conclusion, entrusting me with your medical device application submission would mean gaining access to comprehensive expertise for tailor-made solutions to meet your unique requirements. With Regards! Divya
$750 USD in 7 days
0.0
0.0

This sounds like something I can absolutely deliver ? Clean, professional, user-friendly, and seamless is how I build — no fluff, just results. From smart design to integrated automation, I create systems that look great and work even better. While I’m new to Freelancer, I’ve completed plenty of successful projects off-site with happy clients and real outcomes. I’d love to chat more about your project! Regards, Jarrod.
$400 USD in 14 days
0.0
0.0

We are a global team that is a perfect fit for your project, with extensive experience in regulatory affairs for medical devices. Our team excels in communication with regulatory authorities and has a deep understanding of Thailand's regulatory environment. We offer services including regulatory strategy development and technical documentation preparation. Let's engage about your requirements and we look forward to collaborating with you! Regards, Igshaan
$650 USD in 14 days
0.0
0.0

Nice to meet you sandriner2, It is a pleasure to communicate with you. My name is Anthony Muñoz, I am the lead engineer for DSPro IT agency and I would like to offer you my professional services. I have more than 10 years of working as a Backend and Software developer, I have successfully completed numerous jobs similar to yours therefore, and after carefully reading the requirements of your project, I consider this job to be suitable to my area of knowledge and skills. I would love to work together to make this project a reality. I greatly appreciate the time provided and I remain pending for any questions or comments. Feel free to contact me. Greetings
$972 USD in 7 days
0.0
0.0

Hello I have thoroughly reviewed your project description and am confident in my ability to assist you in completing it successfully. I believe it would be highly beneficial to delve deeper into the specifics of the job to determine the most effective way forward. I am open to scheduling an interview at your convenience, and I genuinely appreciate the chance to collaborate with you on this project. Your response is eagerly anticipated, and I'm excited about the prospect of working together. Thank you for considering my proposal. Looking forward to your prompt reply! Best regards Neha!!!
$750 USD in 7 days
0.0
0.0

I combine deep technical expertise with practical compliance experience, making me uniquely qualified to guide your organization through PCI DSS audit preparation, assessment, and remediation. Certified Cybersecurity Expert – I hold advanced certifications including CCSP, SSCP, Security+, CySA+, and PenTest+, proving both my technical and governance-level expertise in securing cardholder data environments (CDEs). Hands-On Security Management – As an Information Systems Manager, I’ve led end-to-end compliance initiatives, from gap analysis to remediation and revalidation, ensuring that controls meet both PCI DSS and broader security framework requirements. Comprehensive Approach – I don’t just run checklists. I perform thorough risk assessments, map controls to your unique environment, and provide actionable, prioritized remediation plans that minimize operational disruption. Technical & Policy-Level Remediation – I can address both infrastructure security gaps (network segmentation, encryption, vulnerability management) and governance shortfalls (policies, incident response plans, evidence documentation). Proven Audit Preparation Success – My approach ensures your PCI auditor receives clear, well-documented evidence, reducing the likelihood of findings and streamlining the certification process.
$525 USD in 7 days
0.0
0.0

I have worked as a Medical Device scientist and department director, I have 4 years of experience writing scientific reports and presentations for FDA submission. I have expertise in medical device applications in the USA, especially for cardiovascular, endovascular, neurovascular, dermal, metabolic and respiratory therapeutic areas.
$500 USD in 7 days
0.0
0.0

Bangkok, Thailand
Member since Aug 13, 2025
₹1500-12500 INR
₹600-1500 INR
$15-25 USD / hour
₹1500-12500 INR
₹600-1500 INR
€12-18 EUR / hour
$15-25 USD / hour
$15-25 CAD / hour
£10-15 GBP / hour
$8-15 USD / hour
£3000-5000 GBP
₹12500-37500 INR
$250-750 USD
min $50 USD / hour
€12-18 EUR / hour
₹600-1500 INR
€250-750 EUR
$10-30 USD
₹100-400 INR / hour
$30-250 NZD