Kane Biotech Announces Agreement to Acquire FB Dermatology
12 nov. 2024 13h08 HE
|
Kane Biotech Inc.
WINNIPEG, Manitoba, Nov. 12, 2024 (GLOBE NEWSWIRE) -- Kane Biotech Inc. (TSX- V:KNE; OTCQB:KNBIF) (the “Company”, “Kane Biotech”) announces today that it has entered into a binding term sheet (the...
CytoSorbents Submits Health Canada Medical Device License Application for DrugSorb-ATR Following MDSAP Certification
04 nov. 2024 07h00 HE
|
CytoSorbents
CytoSorbents submits DrugSorb-ATR Medical Device License Application to Health Canada following MDSAP Certification. Expects regulatory decision in 2025
Kane Biotech Announces Distribution Agreement with Qatar Datamation Systems for revyve™ Antimicrobial Wound Gel
28 août 2024 08h40 HE
|
Kane Biotech Inc.
WINNIPEG, Manitoba, Aug. 28, 2024 (GLOBE NEWSWIRE) -- Kane Biotech Inc. (TSX- V:KNE; OTCQB:KNBIF) (the “Company” or “Kane Biotech”) today announces that it has signed a three year distribution...
Kane Biotech Announces Distribution Agreement with Razan Medical Trading for revyve™ Antimicrobial Wound Gel
22 août 2024 08h30 HE
|
Kane Biotech Inc.
WINNIPEG, Manitoba, Aug. 22, 2024 (GLOBE NEWSWIRE) -- Kane Biotech Inc. (TSX- V:KNE; OTCQB:KNBIF) (the “Company” or “Kane Biotech”) today announces that it has signed a three year distribution...
Kane Biotech Receives ISO 13485:2016 MDSAP Quality Certification
17 juil. 2024 08h30 HE
|
Kane Biotech Inc.
WINNIPEG, Manitoba, July 17, 2024 (GLOBE NEWSWIRE) -- Kane Biotech Inc. (TSX-V:KNE; OTCQB:KNBIF) (“Kane Biotech” or “Kane”) announces that it has received ISO 13485:2016 Medical Device Single Audit...
MedReg 2023: Annual Medical Device Regulatory Confex - Unveil the Future of Regulatory Compliance
16 août 2023 07h48 HE
|
Research and Markets
Dublin, Aug. 16, 2023 (GLOBE NEWSWIRE) -- The "MedReg 2023 - Annual Medical Device Regulatory Confex" training has been added to ResearchAndMarkets.com's offering. Step into the realm of...
6-Hour Virtual Seminar on Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan (August 11, 2021)
29 juin 2021 04h38 HE
|
Research and Markets
Dublin, June 29, 2021 (GLOBE NEWSWIRE) -- The "Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan"...
bioLytical Laboratories Earns MDSAP Certification, Highest Quality Standard in Medical Device Industry
21 févr. 2019 17h00 HE
|
bioLytical Laboratories Inc.
RICHMOND, British Columbia, Feb. 21, 2019 (GLOBE NEWSWIRE) -- bioLytical Laboratories, a world leader in the development and manufacture of rapid infectious disease tests, is pleased to announce...
bioLytical Laboratories Earns MDSAP Certification, Highest Quality Standard in Medical Device Industry
21 févr. 2019 09h00 HE
|
bioLytical Laboratories Inc.
RICHMOND, British Columbia, Feb. 21, 2019 (GLOBE NEWSWIRE) -- bioLytical Laboratories, a world leader in the development and manufacture of rapid infectious disease tests, is pleased to announce...