Dr. Christopher Joseph Devine, President, Devine Guidance International
Devine Guidance

Inspection: No Signatures Equals a Big Problem

By Dr. Christopher Joseph Devine

…C. (2013). Devine guidance for managing key attributes of a FDA-compliant quality management system – 21 CFR, Part 820 Compliance. Charleston, SC: Amazon. FDA. (June 2016). Inspections, Compliance, Enforcement, and…

…C. (2013). Devine guidance for managing key attributes of a FDA-compliant quality management system – 21 CFR, Part 820 Compliance. Charleston, SC: Amazon. FDA. (June 2016). Inspections, Compliance, Enforcement, and…

Continue reading

Global Revenue Drops, MedTech Struggle for Growth Signals Industry Shift

By Maria Fontanazza

…we look at 2016 and it comes to completion, we’ll see a pretty impressive growth number.” Shareholder-friendly actions. Many companies have focused on stock buybacks and enhancing dividends, all while…

…we look at 2016 and it comes to completion, we’ll see a pretty impressive growth number.” Shareholder-friendly actions. Many companies have focused on stock buybacks and enhancing dividends, all while…

Continue reading

FDA

Software as a Medical Device Draft Guidance Aims for Global Harmonization

By MedTech Intelligence Staff

…“Global regulators expect that clinical evaluation and the evidence generated for a SaMD have the same scientific level of rigor that bis commensurate with the risk and impact of the…

…“Global regulators expect that clinical evaluation and the evidence generated for a SaMD have the same scientific level of rigor that bis commensurate with the risk and impact of the…

Continue reading

Joachim Schaefer
Soapbox

Medtech Trends: Digitization, Smart Technologies and 3-D in the OR

By Joachim SchƤfer

communication technology, medical furniture and specialist furnishings for hospitals and physicians’ offices. The COMPAMED trade fair will be held concurrently with MEDICA. With 18,800 visitors last year, COMPAMED broke its…

communication technology, medical furniture and specialist furnishings for hospitals and physicians’ offices. The COMPAMED trade fair will be held concurrently with MEDICA. With 18,800 visitors last year, COMPAMED broke its…

Continue reading

Brian Williams, PwC

Transformation of New Healthcare Model Demands More Medtech Partnerships

By Maria Fontanazza

…medtech companies are software companies, app developers or consumer-focused companies. There are new entrants with well-developed skills that lack the clinical insight and capabilities medtech companies offer. By collaborating and…

…medtech companies are software companies, app developers or consumer-focused companies. There are new entrants with well-developed skills that lack the clinical insight and capabilities medtech companies offer. By collaborating and…

Continue reading

Dr. Christopher Joseph Devine, President, Devine Guidance International
Devine Guidance

Pins and Needles

By Dr. Christopher Joseph Devine

…reviewed product labeling for the SkinPen II, including your firm’s websites located at http://bellusmedical.com/products/skinpen, http://skinpen.com/ and https://www.youtube.com/watch?v=zWRwhi9Yjrc, brochures, and pamphlets, which revealed that the SkinPen II is an automated, non-surgical…

…reviewed product labeling for the SkinPen II, including your firm’s websites located at http://bellusmedical.com/products/skinpen, http://skinpen.com/ and https://www.youtube.com/watch?v=zWRwhi9Yjrc, brochures, and pamphlets, which revealed that the SkinPen II is an automated, non-surgical…

Continue reading

Ameing for Asia

Chinese Clinical Trials: New GCP Requirements

By Ames Gross

…to the composition and responsibilities of the ethics committee. According to Article 30, there must be at least five members of the committee (with both genders represented) of both medical…

…to the composition and responsibilities of the ethics committee. According to Article 30, there must be at least five members of the committee (with both genders represented) of both medical…

Continue reading

Medical devices market in Russia, Intertek

Five Steps to Medical Device Commercialization

By Michael Lynch

…case of a 510(k) or PMA, the associated fee. After submission, the FDA will conduct an administrative review to determine if the submission is sufficiently complete. FDA staff will communicate…

…case of a 510(k) or PMA, the associated fee. After submission, the FDA will conduct an administrative review to determine if the submission is sufficiently complete. FDA staff will communicate…

Continue reading

ICU Medical to Acquire Hospiraā€™s Infusion Systems for $1 Billion

By MedTech Intelligence Staff

…infusion systems business includes IV pumps, solutions and devices. The union is expected to create a pure-play infusion therapy company, competitive in the U.S. and global market (with direct operations…

…infusion systems business includes IV pumps, solutions and devices. The union is expected to create a pure-play infusion therapy company, competitive in the U.S. and global market (with direct operations…

Continue reading