Medical Device Ceo
Looking for a medical device ceo in ophthalmology.
Looking for a medical device ceo in ophthalmology.
We are in the process of potentially pursuing an opportunity in the medical diagnostic laboratory industry. Target business characteristics: · has 400+ tests and serves over 3,000 physician and hospitals · will complete more than 270,000 patient order in 2017 · testing categories include routine testing and esoteric testing o routine testing is predominantly basic blood analysis and accounts for 60% of volume o esoteric testing accounts for 40% of volumes competitive landscape: · heavily consolidated at the top and highly fragment at the bottom o major players include medlabs, labcorp, quest · industry is not driven by price we are looking for an experienced operator and/or industry executive who can give us insights on (i) reimbursement rate environment; (ii) barriers to entry; (iii) industry success factors; (iv) dynamic between hospital completing testing in-house vs outsourcing; and (v) any upcoming legislation that may significant impact the industry.
Hi sir this is raja from andhrapradesh, india. I want to start a medical disposal syringe unit . For this purpose may i know details about invest amount and how to get machinery details and market potential and all .Is there any consultancy services which is offers services? Please inform me the full details about this project thank you sir.
Joseph | ----------------Director---------------
Zib5e448 Here are initial generic proposals on a direct labor control system that offers up to 40% ...1.5 Hours Later
Hi Raja, I can help you n this, we are based out of Mumbai and have relevant expertise. Regards, ...14.1 Hours Later
A K |Zintro Expert
contact ***** A K Singh...17.1 Hours Later
This is an opportunity for a dedicated medical professional to join our mission of protecting human research subjects as a board chair in our puyallup, washington location. Please note: we are seeking to hire a full-time employee and are not interested in responses from those only interested in consulting. Must be authorized to work in usa without visa sponsorship **position summary**: - provide the highest possible support to our ethical review and research safety programs in areas and issues requiring medical training and judgment. This most commonly involves the institutional review board, and may also include providing medical advice to biosafety committees. **essential duties & responsibilities**: - chair board meetings to ensure compliance with federal and state laws as well as our policies and procedures, and facilitate discussion from board members. Provide scientific, ethical and regulatory support and advice to board members - analyze and present protocols and other agenda items at board meetings to facilitate informed decision making. Set standards and role model effective presentation and discussion for all board members. - analyze research submissions, identify problems and issues, collect additional information or request corrections, and draft memoranda. - research, draft, and present reports to the board on a wide range of topics, including but not limited to, investigator misconduct, site visits, fda and sponsor audits of investigators and others, issues involving human subjects, sponsors, and institutions. - advise clients of applicable scientific information and regulations pertaining to human subject research, both orally and in writing. - analyze requests for exemption determinations and provide formal written opinions that proposed projects are exempt from the requirements for irb review or do not require irb review. - provide guidance to clients to help resolve scientific, ethical and regulatory issues and difficulties. - review literature and other materials to keep abreast of developments in the regulatory, legal, and ethical arenas. **educational qualifications**: - md or do - list the medical licenses you currently hold or have held in the u.S **qualifications/experience requirements**: - experience in submitting and/or reviewing clinical trial protocols is strongly preferred. This experience is normally gained while working in the clinical trial industry or as an irb board member. - experience as a member of an medical ethics review board would be relevant. - able to chair board meeting and effectively present information to a diverse group of professionals - six or more years of related clinical experience and/or training, preferred - ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. - knowledge of ms word, ms excel, ms outlook and ms windows. Please note: we are seeking to hire a full-time employee and are not interested in responses from those only interested in consulting. Must be authorized to work in usa. Kindly respond providing a brief summary of your relevant experience and attach your latest resume on zintro.
Hong |Executive director
Hi I am interested in this position, I have over 20 years experience in clinical, medical, et al. I...27 Minutes Later
Dear Sir/Madam, I'd like to be considered for this position. Solid academic background (MD/PhD in Cl...1.3 Days Later
Joseph |Pharmaceutical Consultant
I am a cardiologist with extensive clinical trial experience in both academia and the pharmaceutical...1.6 Days Later
Which of the disposable medical devices has the highest profit margin?
I have some experience with disposable peripherals used with several products I designed for world w...39 Minutes Later
John |Consultant & Executive
I think I can give you a good sense of profit margins. Feel free to contact me. John Stengrevics...42 Minutes Later
Ron |Director, Clinical Marketing
20 years experience both buying and selling disposables. I'd be delighted to help......1.2 Days Later
1. Can you please provide a list of requirements for medical device (health canada class ii & iv) registration in argentina? 2. Is it possible for a canadian company to hold the registration license under their name in argentina? 3. If we cannot hold the license in our name, and we want to change/replace the license holder, do we need to reapply? Please explain the process of replacement of license holder (if applicable). 4. We have contract manufacturers overseas who make our products, but we are the legal manufacturers. Do the free sale certificates have to demonstrate product codes from the contract manufacturer or the legal manufacturer (since our codes are different from the contract manufacturer)? Or, do we have to provide a notarized letter demonstrating equivalency of our product codes to the contract manufacturers codes for each product? (our free sale certificate contains only our product codes). 5. Is the health canada export certificate acceptable in argentina (it does not state our contract manufacturers details)?
Looking for medical device manufacturers in michigan, ohio, wisconsin, minneapolis
What type of capabilities do they need to have? Plastics Molding? Silicone Molding? Metal Fabricatin...24 Minutes Later
I currently provide engineering and *****ulting to medical device companies as well as con...36 Minutes Later
Ali |DFSS MBB
What do you exactly need?...3.1 Hours Later
We are looking for an expert in the area of medical device development, specifically for knowledge in: plasma based therapeutic apheresis column development using antibodies/peptides matrix/antibody coupling options and optimization sterilization processes including aseptic technique versus end-sterilization for these devices knowledge of regulatory issues also a plus.
James |General Manager
Please contact me at *****, as require further ***** response. 20+ years of...1.9 Hours Later
Dear Inquirer: I am a professional with more than 10 years of experience in Life Science product de...2.2 Hours Later
Srinivas |Marketing Manager
Hi, I'm a *****eting executive and product manager experienced in business and product devel...12.1 Hours Later
Repost -- mdb is an authorized zintro partner. Mdb is looking for a ceo and three board members for one of its new start-ups called electroblate, inc. Can you help us fill these positions? If your referral for the ceo position is hired you will earn a reward of $20,000. If your referral for a board position is appointed you will earn $10,000. Note: you are welcome to apply for the positions, but are not eligible for a referral fee for referring yourself. Here is how it works: 1. Submit the candidates (or apply) via the following links: - ceo position: http://bit.Ly/1rxtd43 - board position(s): http://bit.Ly/1wrhraj 2. Within one week you will receive feedback and you will be kept up to date with the progress. Here is a brief description of electroblate and you can learn more by clicking on the links provided above. Electroblate, inc. Is a clinical-stage, medical device company developing a unique platform to induce programmed cell death (apoptosis) in soft tissue non-thermally. By inducing apoptosis the body doesn't recognize injury and repairs the treated tissue with normal tissue in the treated area. The applicable worldwide market, exceeds $15 billion, and targets multiple therapeutic applications, such as tumor/cyst/unwanted tissue ablation, and multiple cosmetic applications. The company is a technology ?Roll-up? Being created by mdb to acquire the operations and ip of three companies and two universities, enabling electroblate a dominant ip position in this technology area. In addition, the principal scientists and inventors are equity holders and will be working with the company to help further the technology platform. Thanks again for your help in our mission of maximizing the probability of success of these disruptive technology companies! best regards, chris
Anna |VP, Managing Director
I am experienced and ***** this role. Please, let me know what ***** that job. I will se...1 Minute Later
Shashi |Executive Vice President
I can help. Pls email at ***** call me at *****. Shashi...1 Minute Later
Bernadette |Director, Consultant
Hello I am an Advanced Practiced Registered Nurse with fifteen plus years of experience in Managed C...1 Minute Later
One of our clients is seeking to learn about the process of medical records retrieval in the p&c insurance industry. If you work at a p&c insurer or have experience consulting for such an organization - are you familiar with the process of attorneys / litigators using third-party records retrieval firms to retrieve medical records for a p&c insurance case? If so - we would love to discuss next steps.
I need a medtech/medical devices expert with a strong history in quality management for manufacturing and operations. Ideally this expert will have a strong understanding of these manufacturing processes, including things like the expected contaminant levels and tolerances in a clean room, etc. The expert would ideally be located in either south california or the east coast (baltimore would be ideal).
We are using a new api as an active ingredient in a coating formulation to be applied to a wide variety of medical devices. The api elutes out slowly over time. Looking to find an expert with tox and regulatory knowledge on combination medical devices (device/drug) spanning many different fields of use: dermatology, vascular access, respiratory, orthopedic and others.