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Frequently Asked Questions (FAQs)

Welcome to our FAQs section. Here, you’ll find answers to common questions about our services and how to contact us. If you have more questions, please use the contact form above.

We provide regulatory guidance, compliance consulting, training, document review, market access support, and more. For a full list of services, please visit our About Us page.

You can contact us via email at support@medtechregulations.com, phone at +256760209747, or by using the contact form on this page.

We specialize in providing regulatory guidance for medical devices in various African countries, and we also offer services globally.

We strive to respond to all inquiries within 1-2 business days.

Yes, we offer personalized consulting services tailored to your specific regulatory needs. Please contact us for more details.

Yes, you can schedule a meeting or consultation by contacting us via email or phone, or by using the contact form on this page.

We offer training programs on ISO 13485 implementation, risk management, quality management systems, and more. Check our Services page for detailed information.

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You can find information on upcoming events and workshops on our Events page. You can also contact us directly for more details.

Yes, we offer customized regulatory pathway guides tailored to your specific medical device and target market. Please contact us with your requirements, and our team will assist you in developing a personalized guide.