124 results on '"Medical supplies -- Product development"'
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2. Futura Medical reports positive developments in product pipeline
3. IRLAB has received approval from the Swedish Medical Products Agency to conduct a Phase I study of the drug candidate IRL757
4. US FDA To Develop Regulatory Scheme For AI In Medical Products, Foster International Cooperation
5. LIB Therapeutics And Partner Hasten Biopharmaceuticals Unveil Lerodalcibep Clinical Trial Application Acceptance by the Center for Drug Evaluation at the National Medical Products Administration in China
6. LIB Therapeutics and Partner Hasten Biopharmaceuticals Announce Lerodalcibep Clinical Trial Application Acceptance by the Center for Drug Evaluation at the National Medical Products Administration in China
7. Provision Of Services To Support Clinical Trials In The Form Of A Comparative Analysis Of Medical Products: instruments And Devices For Osteosynthesis , instruments And Implants For Osteosynthesis , external Fixation Devices 905-u690-24/4
8. GSK's regulatory application for Shingrix for the prevention of shingles in at-risk adults aged 18 and over accepted for review by China National Medical Products Administration | GSK
9. GSK's regulatory application for Shingrix for the prevention of shingles in at-risk adults aged 18 and over accepted for review by China National Medical Products Administration
10. GSK's regulatory application for Shingrix for the prevention of shingles in at-risk adults aged 18 and over accepted for review by China National Medical Products Administration
11. Researchers at Jazan University Target Pulpotomy [Comparative Evaluation of New Needleless Local Anesthetic System (INJEX) and Conventional Syringe Needle Technique during Pulpotomy Treatment: A Randomized Clinical Trial]
12. COLLECTION OF RACE AND ETHNICITY DATA IN CLINICAL TRIALS AND CLINICAL STUDIES FOR FDA-REGULATED MEDICAL PRODUCTS; DRAFT GUIDANCE FOR INDUSTRY
13. Oxford Medical Devices Ltd secures contract for Provision of consultancy and product developments for CAVA medical device and associated software
14. INCREASING OPTIONS IN CLINICAL RESEARCH TO FACILITATE MEDICAL PRODUCT DEVELOPMENT
15. CONSIDERATIONS FOR THE CONDUCT OF CLINICAL TRIALS OF MEDICAL PRODUCTS DURING MAJOR DISRUPTIONS DUE TO DISASTERS AND PUBLIC HEALTH EMERGENCIES
16. The First of Its Kind in the World: The Recombinant Multivalent COVID-19 Protein Vaccine against XBB Variants by WestVac Biopharma|West China Medical Center, Sichuan University has been Approved for Clinical Trials by The National Medical Products Administration of China
17. The First of Its Kind in the World: The Recombinant Multivalent COVID-19 Protein Vaccine against XBB Variants by WestVac Biopharma/West China Medical Center, Sichuan University has been Approved for Clinical Trials by The National Medical Products Administration of China
18. Subcutaneous Immunoglobulin Prefilled Syringe Development Agreement Announced by KORU Medical Systems
19. KORU Medical Systems Announces Subcutaneous Immunoglobulin Prefilled Syringe Development Agreement
20. KORU Medical Systems Announces Subcutaneous Immunoglobulin Prefilled Syringe Development Agreement
21. MODEPHARMA LIMITED secures contract for Contract for the Provision of Clinical Trials Services to the LOCI Trial Manufacture (package, label) and Distribute Investigational Medical Product (IMP) including Placebo to the University of Birmingham (Campaign
22. Hospital Clinic Porto Alegre Details Findings in Fibrin Tissue Adhesives (Autologous Fibrin Glue Versus Sutures for Conjunctival Autograft In Primary Pterygium: a Randomized Clinical Trial)
23. KORU Medical Systems signs SCIg prefilled syringe development agreement
24. KORU Medical Systems signs SCIg prefilled syringe development agreement
25. FDA PATIENT-FOCUSED DRUG DEVELOPMENT GUIDANCE SERIES FOR ENHANCING THE INCORPORATION OF THE PATIENT'S VOICE IN MEDICAL PRODUCT DEVELOPMENT AND REGULATORY DECISION MAKING
26. Mabpharm Limited: VOLUNTARY ANNOUNCEMENT APPROVAL OF CLINICAL TRIAL APPLICATION OF CMAB807X BY THE NATIONAL MEDICAL PRODUCTS ADMINISTRATION OF CHINA
27. Shanghai Henlius Biotech, Inc.: VOLUNTARY ANNOUNCEMENT APPLICATION FOR CLINICAL TRIAL OF HLX35 (RECOMBINANT HUMANISED ANTI-EGFR AND ANTI-4-1BB BISPECIFIC ANTIBODY INJECTION) FOR THE TREATMENT OF ADVANCED MALIGNANT SOLID TUMORS APPROVED BY THE NATIONAL MEDICAL PRODUCTS ADMINISTRATION (Stock code: 2696)
28. Promore Pharma Receives Permits to Start a Phase II Clinical Trial Regarding Scar Prevention
29. China Medical System Holdings Limited: Voluntary and Business Update Announcement Methotrexate Injection, Pre-filled Syringe Granted an Approval for Drug Clinical Trial
30. ImmVira's MVR-T3011 Obtained NMPA's Approval for Intravenous Administration (IV) Phase I Clinical Trial
31. ImmVira's MVR-T3011 Obtained NMPA's Approval for Intravenous Administration (IV) Phase I Clinical Trial
32. Mika Medical, a Korean Manufacturer Specializing in Syringe Technology, Has Completed Clinical Trials with Yonsei University Severance Hospital and Catania University
33. Mika Medical, a Korean Manufacturer Specializing in Syringe Technology, Has Completed Clinical Trials with Yonsei University Severance Hospital and Catania University
34. Shanghai Henlius Biotech, Inc.: VOLUNTARY ANNOUNCEMENT APPLICATION FOR CLINICAL TRIAL FOR RECOMBINANT ANTILAG-3 HUMAN MONOCLONAL ANTIBODY INJECTION HLX26 FOR THE TREATMENT OF SOLID TUMOURS AND LYMPHOMAS APPROVED BY THE NATIONAL MEDICAL PRODUCTS ADMINISTRATION
35. Citrine Medicine Announces Receipt of Clinical Trial Waiver from the National Medical Products Administration (NMPA) in China for Narcolepsy Therapy Wakix(r) (pitolisant) and Partnership With Chinese Alliance for Rare Diseases (CARD)
36. Citrine Medicine Announces Receipt of Clinical Trial Waiver from the National Medical Products Administration (NMPA) in China for Narcolepsy Therapy Wakix (pitolisant) and Partnership With Chinese Alliance for Rare Diseases (CARD)
37. Delivery Of Medical Products For Clinical Trials For The State Healthcare Institution 'tula Regional Clinical Hospital'
38. CORONAVIRUS (COVID-19) UPDATE: FDA CONTINUES IMPORTANT WORK TO SUPPORT MEDICAL PRODUCT DEVELOPMENT TO ADDRESS NEW VIRUS VARIANTS
39. Marinus Enrolls First Patient in Pivotal Phase 3 Clinical Trial of IV Ganaxolone in Refractory Status Epilepticus
40. EdiGene Announces Approval of its IND Application for its CRISPR|Cas 9 Gene-editing Hematopoietic Stem Cell Therapy ET-01 in b-thalassemia by China National Medical Products Administration
41. EdiGene Announces Approval of its IND Application for its CRISPR/Cas 9 Gene-editing Hematopoietic Stem Cell Therapy ET-01 in -thalassemia by China National Medical Products Administration
42. Shanghai Henlius Biotech, Inc.: VOLUNTARY ANNOUNCEMENT APPLICATION FOR CLINICAL TRIAL FOR RECOMBINANT ANTI-CD38 HUMAN MONOCLONAL ANTIBODY INJECTION (HLX15) FOR THE TREATMENT OF MULTIPLE MYELOMA APPROVED BY THE NATIONAL MEDICAL PRODUCTS ADMINISTRATION (Stock Code: 2696)
43. Plan ahead for combo device success: the best combination medical device makers select product materials, process steps, and monitoring strategies in the early stages of product development to ensure biocompatibility and product stability throughout the manufacturing process
44. Shanghai Henlius Biotech, Inc.: VOLUNTARY ANNOUNCEMENT APPLICATION FOR CLINICAL TRIAL FOR RECOMBINANT ANTI-CD38 HUMAN MONOCLONAL ANTIBODY INJECTION (HLX15) FOR THE TREATMENT OF MULTIPLE MYELOMA ACCEPTED BY THE NATIONAL MEDICAL PRODUCTS ADMINISTRATION (Stock Code: 2696)
45. FDA OFFERS GUIDANCE TO ENHANCE DIVERSITY IN CLINICAL TRIALS, ENCOURAGE INCLUSIVITY IN MEDICAL PRODUCT DEVELOPMENT
46. Everest Medicines Limited: VOLUNTARY ANNOUNCEMENT BUSINESS UPDATE ON APPROVAL OF CLINICAL TRIAL APPLICATION BY CHINA NATIONAL MEDICAL PRODUCTS ADMINISTRATION FOR PHASE 3 REGISTRATION TRIAL OF TRODELVYTM FOR METASTATIC BREAST CANCER IN CHINA (Stock Code: 1952)
47. Everest Medicines Announces Approval of Clinical Trial Application by China National Medical Products Administration for Phase 3 Registration Trial of Trodelvy(TM) for Metastatic Breast Cancer in China
48. EdiGene Announces IND Application for its CRISPR|Cas 9 Gene-editing Hematopoietic Stem Cell Therapy ET-01 in b-thalassemia Accepted for Review by China National Medical Products Administration
49. EdiGene Announces IND Application for its CRISPR/Cas 9 Gene-editing Hematopoietic Stem Cell Therapy ET-01 in -thalassemia Accepted for Review by China National Medical Products Administration
50. FDA Issues Guidance on Conduct of Clinical Trials of Medical Products During COVID-19 Pandemic
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