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The BPCDX manufacturing process and device test results presented here, along with preclinical data and pilot clinical results at 6–12 months of follow-up, were submitted to Regulatory Authorities in Sweden (Medical Products Agency) and the Czech Republic (State Institute for Drug Control), and approvals were granted for a randomized controlled study protocol according to EU Directive 93/42/EEC on Medical Devices (decision 5.1-2018-44565, Sweden
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"BPC 157 and wound healing: New perspectives in soft tissue injury management." Injury , 51(1), S45–S54
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