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  1. 1. Provide a clear description of your needs and your expectations of an expert, consultant or job candidate and Zintro will match it with the most relevant professionals in our platform.
  2. 2. Within a day or two typically 6 - 12 Experts, who have opted-in, will contact you with a brief explanation of their qualifications and how they can help.
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Recent Generic Drug Inquiries

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Pharmaceutical Generics Drugs

We're looking for a consultant who is very familiar with the italian pharmaceutical generics market.

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    Stefano |Head of CMC

    I am an italian consultant and could provide support on the topic, best regards, Stefano Biondi...

    1.5 Hours Later
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    Richard |Principle... Independent Contract Consul

    Hello: I received this yesterday. I have general experience in Italy as well as the Caribbean. Pleas...

    1 Day Later
+2 Other Responses
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Generic And Patented Drugs In Europe

Hi, i am looking for distribution mark-up of generic and patented drugs in europe regards, arun

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    Shaun |Vice President

    Hi Arun I can help, can you give more details as to the drug types and manufacturers? Is it all eea ...

    3 Hours Later
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    Yevgen |Scientific Director

    Hello. I\m Expert in pharma distribution in Europe. Can help...

    17.2 Hours Later
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    Samer |Pharamcist

    as a canadian pharmacist, I could help...

    3.1 Days Later
+7 Other Responses
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Bioequivalence

Hi, iam dayo akinwale, the chair/president/ceo, of "ondo pharmaceutical co,inc., in palm beach, florida, united states of america. I am submitting "anda (abr. New drug application) to the u.S. Food and drug administration, for approval to manufacture generic drugs. I am in need of bioequivalence experts, companies who can write be. To approve anda application, be must be proved that the generic drug(s) is equivalent to innovator (brand drugs). I will be grateful, if you contact me through zintro. Sincerely, dayo

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    Clifford |President

    I am an expert in BE studies and ANDAs. I have conducted >50 BE studies and played a pivotal roll in...

    6 Minutes Later
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    Donald |President, Pharmaceutical Research Servi

    I have been involved in designing protocols and setting up of clinical sites to conduct bioequivalen...

    34 Minutes Later
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    Ram |CEO-Founder

    We can assist. Ram Balani...

    48 Minutes Later
+13 Other Responses
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Pharmaceutical Pricing

Looking for experts in generic drug pricing distribution

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    Alan |Director, Provider Relations

    I have over 16+ years experience in Generic Drug Pricing along with pharmaceuticals pricing....

    4 Minutes Later
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    Lisa |President & CEO

    Med-eHUB specializes in health payment systems and in particular, pharmaceutical payment. Please fee...

    59 Minutes Later
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    Michael |Principal

    I have *****ncial proposals from vendors to payers for nearly 20 years. This includes reta...

    2.9 Hours Later
+7 Other Responses
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Pharma Formulation

Formulation development consultant for pharma industry with 12 to 14 years experience in nce and generics drug product development

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    Leah |Managing Partner

    We have a small consulting group focused on drug product development. I have 20+ years in formulati...

    43 Minutes Later
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    Anthony |Independent Consultant

    I am a well-trained scientist (Ph.D., Biochemistry) in the Albuquerque, NM area with a strong backgr...

    1.1 Hours Later
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    Jisheng |Season Professional in pharmaceutical fo

    With 12 years experience in generic pharmaceutical product development, I am very interested in your...

    1.7 Hours Later
+7 Other Responses
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Medical Distributors & Private Labels

We are a u.S.-based consulting firm doing research on medical distributors and private label products. Specifically, we need expert opinion/information on how mckesson and similar medical distributors chooses whether or not to manufacture a private label version of a product. Specifically, i am looking for the volume threshold and other specific factors that drive this decision. Please only send a response if you have been an employee of mckesson or a similar distributor or you have been an employee of a company whose product mckesson decided to private-label, or you have been an employee of a private label manufacturer. Also, please only send a response if you can give up-to-date, specific information. You don't need to include the specific information in your response, of course. However, i am not looking for general guidelines and high-level strategic understanding. I'm looking for specific volume thresholds and other concrete criteria.

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    New |

    Our Company Heisuke Electric and Heavy Industries is in search of a competent individual or firm tha...

    4.3 Hours Later
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    Polina |Oversight & Monitoring Lead, Health Care

    I have worked with McKesson for a product which it decided to ***** ownership partnership...

    4.4 Hours Later
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    Jose |Vice President - Regulatory Affairs and

    This is my specialty - regarding the ********** requirements to sell/distribute pri...

    1 Day Later
+5 Other Responses
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Generic Pharmaceuticals Market In India

We are a global consulting firm currently working on a mandate in the indian generic drugs space. We are looking to connect with experts having extensive prior experience in the strategy, commercial and r&d functions of indian generic manufacturers with presence in usa retail market and having own api manufacturing setup. Please respond with your relevance to this request and your availability for a paid phone consultation this week.

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    Vijayaraghavan |Premier Expert Consultant

    Hello this is Dr V Srini Srinivasan former Chief Science Officer and Executive VP at the Zunited Dt...

    39 Minutes Later
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    Hector |Consultant

    I am a professional from Pharmaceutical Industrial area, with experience since 1992, and more th...

    58 Minutes Later
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    Srinivas |Chief Executive Officer

    Please send your requirements to ***** ...

    1.4 Hours Later
+31 Other Responses
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Pharmaceutical R&d Lab In New York

I have a client in suffolk county, long island, new york that wants to establish a pharmaceutical r&d lab to develop generic drugs, with the goal of manufacturing in the future. I would like to find one or two consultants servicing long island who are familiar with the permitting process for such labs (fda, epa, nysdec, etc).

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    Mary |President, Microbiology Network Inc.

    I am certainly able to assist with this effort as it is one I have done several times in the past. ...

    1.2 Hours Later
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    Michael |Senior Principal Consultant

    I would love to assist in this exciting project to establish an R&D lab and possibly a manufacturing...

    1.2 Hours Later
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    Nathan |Sole Proprietor

    I was EHS supervisor at Pfizer in Brooklyn NY and am familiar with DEC and EPA permitting. I work wi...

    1.3 Hours Later
+14 Other Responses
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Indian Generic Drugs Space

We are a global consulting firm currently working on a mandate in the indian generic drugs space. We are looking to connect with experts having extensive prior experience in the strategy, commercial and r&d functions of indian generic manufacturers with presence in usa retail market and having own api manufacturing setup. Experience/knowledge of the following topics: - emerging and high growth areas (therapeutic areas or api product type) in the api space in india and other emerging markets, the us and european market. - capabilities required to succeed in specific markets and specific therapeutic areas. - overview on key players in api generics space and various business models adopted by large, midsize and small players (e.G., api focus with formulation add-on's, therapeutic area focus). Please respond with your relevance to this request and your availability for a paid phone consultation this week.

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    Karthik Arun |Head, Healtchare Research & Consulting

    I have worked with one of the top Indian API producers in the business development function. The com...

    23.1 Hours Later
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    Prateek |Global Clinical Project Manager

    I have worked with many top Indian API producers in field of Clinical Research and BA/BE studies...

    23.4 Hours Later
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    Pradeep |Commercial Director- Pharmaceuticals

    Having handled Generics as well as brands in Europe and Asia Pacific as management board director of...

    23.6 Hours Later
+20 Other Responses
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Generic Drug

We look for a consultant who is an expert in generic drug regulations, particularly for the generic drug that requires bio-ind for bio-equivalence studies; who is able to make strategic plan for the assembly of the bio-ind package and guide the communication with us fda.

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    Lola |Vice Presidentt and Strategic Developmen

    Hi I don't need to google Bio-IND to know about generic drugs o r what it is - sorry if my comments...

    1.1 Days Later
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    Rita |Principle

    you can reach me at ***** at *****...

    5.1 Days Later
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    Jukka |President, Director

    I have years of experience in generic drug development and have full understanding of *****. I...

    6.7 Days Later
+8 Other Responses
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Clinical Research Organization (cro)

**please respond to the following request with a proposal if: 1) you currently, or within the last year, work at a pharmaceutical or biotech firm. 2) you are familiar with phase 1 clinical trials. Familiarity with and understanding of how biopharma and pharmaceutical companies decide which cros to use for early stage phase 1 clinical research. Will be able to speak to growth trends related to spending on r&d in industry and spending on cro services. To the extent possible, will be able to speak to how this may differ for innovator versus generic drugs. Will be able to speak to the reputations of different cro service providers for early stage phase 1. 1) how has your spending on cro early stage services trended in the past few years? What is your outlook for demand for cro services? Why? To the extent you can speak to this, how has this differed for generic vs. Innovator drugs? 2) what is the decision process for determining which early stage phase 1 cro to use? 3) what factors are considered when determining which early stage phase 1 cro to use? 4) what are the early stage phase 1 cros that come to mind? Which cros have you considered? How do cro reputations differ across the different stages of clinical research (early vs. Late)? For different clinical services? 5) what are the trends for early stage phase 1 cro services moving overseas? Areas of expertise: seeking experts with knowledge of clinical trials, phase 1-4; clinical trials; early clinical research; cro; early stage clinical research; cros; clinical research organization; clinical research

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    Insynergy |Executive Director, Clinical Trials.

    Hi, I'm expert in Phase I clinical research, I received this request many times. I'm so sorry that I...

    3.5 Hours Later
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    Rishit |Executive

    How can I help you? Dr. Rishit...

    16.8 Days Later
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    Jill |Director Project Management, Director Bu

    I sent your question to an ***** may be able to help you. Best regards, Jill...

    19.8 Days Later
+7 Other Responses
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Generic Drug Patenting

We are seeking a phone interview with an ex-executive/manager of novartis pharmaceuticals or sandoz. This person must have knowledge regarding the following questions: 1. Does sandoz (the generics division) operate completely independently from the pharmaceuticals division? 2. Product life cycle – when are off-patent products transferred from the pharmaceuticals division to sandoz? 3. Does novartis pharmaceuticals have products that compete with each other? How is this competition managed? 4. Sandoz r&d budget – is the budgets dedicated only to the development of third party products or does sandoz also invest in developing competing novartis products? 5. Do novartis and sandoz market and sell their portfolio separately or jointly?

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    Polina |Oversight & Monitoring Lead, Health Care

    I have consulted with Sandoz genetics and can speak to their product investment and development appr...

    1.8 Hours Later
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    Sam |Sr. Project Manager, Program Manager, Di

    No, It does not!!!! Although it is one of their biggest branches, its not a profit making unit like ...

    1.1 Days Later
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    John |Consultant

    Try *****....

    1.1 Days Later
+7 Other Responses
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