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There are 1,000 companies in the field of Biopharma on spotfolio that produce or deliver products, that utilize or research technologies or that are otherwise engaged in topics such as Clinical, Drug, Patients, Research, Treatment, Pharmaceutical, Therapeutic, Disease, Study .

Start-ups (155)

Early-stage companies (267)

Established companies (503)

The majority of these companies is located in the following countries.

United States (513)

United Kingdom (78)

China (48)

Canada (46)

Example Companies

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Zivo Bioscience HEALTH ENHANCEMENT PRODUCTS INC

established

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- Project Updates - Presentations Poultry Pen Study Repeat Scheduled for Late July Poultry Pen Study Repeat Scheduled for Late July Jul 12, 2018 ZIVO ...

a poultry pen study in May/June timeframe to establish inclusion rates of ZIVO product in broiler feed. Results from the poultry pen study proved inconclusive ...

inconclusive, spurring a detailed analysis of the entire study. The poultry pen study followed three (3) successful poultry cage studies. There are significant ...

differences in the design of each type of study. The cage studies utilized 300-400 birds each, while the pen study utilized about 3,000 in total. The length ...

length of the cage studies was 28 days, in contrast to the pen study, which ran to 42 days. There were also differences in how the feed was processed and ...

a repeat study was necessary to account for variables that were not addressed in the transition from cage study to pen study. The repeat study is to commence

biotech/agtech R&D company has commenced a third in vivo dairy cow mastitis study to validate its bioactive compounds in combating a specific infective pathogen ...

including the landmark study that indicated efficacy of ZIVO bioactives in combatting a drug-resistant pathogen. The current study is focused on establishing ...

subsets that tested one or two variables at most. The results of this current study will be shared with collaborators and researchers working on the analytical ...

required extensive testing and screening to assure healthiness before the study commenced and to acclimate successfully to its new surroundings at the research ...

number of cows recruited for the study could not pass the health exams or successfully adapt to new surroundings, the study would have been delayed until ...

test samples arrived on time, and the study commenced immediately thereafter. The duration of the active study is roughly 4 weeks, following by extensive

WCG

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Case Study Case Study PharmaSeek COVID-19 Case Study Case Study How a Top 25 Pharma Company Reduced the Placebo Response for their Phase II Study Case ...

Case Study How a Top 20 Pharma Company Protected Their Primary Endpoint Case Study How A Top-Pharma Client Transformed Its Safety-Reporting Process, ...

in One Year Case Study WCG iConnect— University of Pennsylvania Case Study WCG ThreeWire— Endometriosis Case Study Case Study: Retrospective Endpoint ...

Committee Case Study WCG ThreeWire– Oncology Study Case Study WCG ThreeWire– UC Crohn's Study Case Study WCG ThreeWire– Vaccine Study for Top 10 Pharma ...

Pharma Case Study WCG ThreeWire– Psoriatic Arthritis Case Study How Celgene Transformed Its Safety-Reporting Process, Saving $5.7 million In One Year ...

Year Case Study Accurate Pain Reporting WCG Analgesic Solutions found that patients could better report their pain intensity and discriminate between active

subjective endpoints during the COVID-19 pandemic.View - Services - Study Planning & Site Optimization - Benchmarking & Analytics - Site Selection ...

Recruitment & Retention - eCOA / ePRO - Timely, Targeted Interventions - Study Insight Analytics - Scientific & Regulatory - Trial Design and Protocol ...

Ethical & Biosafety Review - WCG IRB WCG IRB DIVISION - Solutions - Study Fast-Start - Enrollment360 - PrecisionCNS - Oversight & Safety - SiteReady ...

eResearch - Velos eResearch eXpress - CenterWatch iConnect - ConsentNow - Study Insight Analytics - eCOA/ePRO Platform - SafetyPortal™ - WCG Institute ...

your biggest challenge? Back - COVID-19 Resource Center - Services - Study Planning & Site Optimization - Site Selection - Site Feasibility - Site ...

Patient Identification - Recruitment & Retention - CenterWatch iConnect - Study Marketing - Rater Services - ConsentNow - Scientific & Regulatory -

Dermelix Dermelix Biotherapeutics

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Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information. x Skip to Main ...

How to Use Search Results - How to Find Results of Studies - How to Read a Study Record - About Studies - Learn About Studies - Other Sites About Studies ...

Rule - How to Apply for a PRS Account - How to Register Your Study - How to Edit Your Study Record - How to Submit Your Results - Frequently Asked Questions ...

How to Use Search Results - How to Find Results of Studies - How to Read a Study Record - About Studies - Learn About Studies - Other Sites About Studies ...

Rule - How to Apply for a PRS Account - How to Register Your Study - How to Edit Your Study Record - How to Submit Your Results - Frequently Asked Questions ...

Conditions - Disclaimer - PRS Login - Home - Find Studies - How to Read a Study Record Saved Studies Find Studies - Search - Advanced Search - See Studies

Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information. x Skip to Main ...

How to Use Search Results - How to Find Results of Studies - How to Read a Study Record - About Studies - Learn About Studies - Other Sites About Studies ...

Rule - How to Apply for a PRS Account - How to Register Your Study - How to Edit Your Study Record - How to Submit Your Results - Frequently Asked Questions ...

How to Use Search Results - How to Find Results of Studies - How to Read a Study Record - About Studies - Learn About Studies - Other Sites About Studies ...

Rule - How to Apply for a PRS Account - How to Register Your Study - How to Edit Your Study Record - How to Submit Your Results - Frequently Asked Questions ...

public. Each study record includes a summary of the study protocol, including the purpose, recruitment status, and eligibility criteria. Study locations and

Seranovo

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Feasibility Study Formulation Development Preclinical Trial Material production GMP production 1. 2. 3. 4. Feasibility Study In a feasibility study, we first ...

polymeric precipitation inhibitors. The key deliverable of a feasibility study is a report with clear conclusions and recommendations for follow-up work ...

feasibility study requires 2 g of API and is completed in 8 weeks. Formulation Development Building further on the results of the feasibility study, we continue

Lateral Pharma

early-stage

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Lateral Pharma commenced its first clinical study, LAT-NP-001, in Q1 2019. LAT-NP-001 is a Phase IIa study of the efficacy and safety of twice daily oral ...

placebo-controlled, crossover study. Patients were recruited from four sites across Australia and two in the United Kingdom. Having reached its study target in Q1 2020 ...

the study was closed to recruitment, and results will be available by Q3 2020. LAT-MIG-001 Lateral Pharma commenced its second clinical study, LAT-MIG-001 ...

LAT-MIG-001, in Q3 2019. LAT-MIG-001 is a proof-of-concept Phase IIa study of the efficacy of oral LAT8881 in acute migraine. There were 21 patients with acute ...

placebo-controlled, crossover study. Patients were recruited from three sites across Australia. Having reached its study target in Q2 2020, the study was closed to recruitment

first clinical study, LAT-NP-001, in Q1 2019. Read More Acute migraine (LAT-MIG-001) Lateral Pharma commenced its second clinical study, LAT-MIG-001,

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