Global Clinical Trials (GCT) United States

Global Clinical Trials (GCT) is a premium contract-research organization (CRO) that offers support for the clinical Phase I-IV studies as well as post-marketing activities to Big Pharma, small and medium-sized biotech enterprises, groups and funds, as well as large universities and institutions. Headquartered in Princeton, USA, GCT offers both local and global support through 10 own operational offices in Bulgaria, Czech Republic, Georgia, Hungary, India, Kazakhstan, Latvia, Lithuania, Estonia, Moldova, Poland, Romania, Russia, Slovakia, Ukraine.
GCT team, that now consists of over 100 full-time clinical research professionals, gives individualized attention to each project and provides full range of services following the latest GCP, EMA and FDA guidelines at every stage of product development path. Our monitors and project managers are all certified clinicians experienced in GCP clinical research. Our experience, competent staff, close contact with the KOLs and the immense enrollment potential of the covered region ensure fast study start-up and compliance with the set timelines.
GCT owns 400 sq.m. (4300 ft2) Drug Storage and Distribution facility in St. Petersburg, Russia. It is fully equipped, disaster protected and has multiple modes of storage (ambient, climate controlled, refrigerated, frozen). High standards of work and client satisfaction are proved by the fact that more than 80% of the business come from repeat clients.
Since 2006 GCT is also an Exclusive Partner of “The White Nights” International ophthalmology congress in Russia.
Company Size (Fulltime employees)
Year of foundation
2001
Stock Market and Ticker/Symbol/Number
N/A
Please specify your partnering goal
Networking, new business opportunities
Headquartner in China
Plan in China
GCT is looking for potential new business opportunities, offering full-service clinical trials support worldwide for Chinese pharma companies.
Biotech/Pharma Category
Biotech/Pharma Asset Stage
Medtech Development Stage
Your Service Name
clinical trials, market authorization, registration, consulting
Service Description
logistics, regulatory services, project and site management, pharmacovigilance, medical monitoring, data management, biostatistics, medical writing, GDPR and DPO, EU Legal representation,
Target Client Type
Pharma, Biotech, Device companies
Aleksandr Stiblo
LinkedIn logo Director, Business Development 
Functionality

GlycoSeLect Ltd Ireland

Our company develops and manufactures technology and applications for glycoprotein separation and analysis. We are focussed on the biopharmaceutical industry. We also have customers in medical diagnostic and cosmetic companies.
Our facility is based on the campus of Dublin City University in Ireland.
We have developed an extensive network of contacts not only customers but also opinion leaders in glybiology.

Website:
GlycoSeLect Ltd
Company Size (Fulltime employees)
Year of foundation
2013
Please specify your partnering goal
Joint venture to develop downstream processing applications
Funding Status
Series A
Now raising (In USD)
900,000
Headquartner in China
Plan in China
Seek local partner to establish glycobiology specialist company supplying better glycoprotein product analysis and manufacturing technology with support for application development.
Biotech/Pharma Category
Assets Information 1: Name|Description|Indications|Stage|IP countries
RPL lectins for glycoprotein product analysis & manufacturing applications|Glycan specific proteins for use in detecting and separating glycoproteins|Product analysis and manufacturing, especially vaccines and mAbs.|Worldwide available
Biotech/Pharma Asset Stage
Slides Deck
(pdf, 164.08KB)
Robert Dunne
CEO 
Functionality

Golden State Green World United States

Golden State Green World LLC, is a CBG Hemp Cultivator, located in Riverside County, California. Our team has ten years of extensive greenhouse design and a diverse growing experience. We apply our grow methodologies and eco-agricultural knowledge to supply the global market with high quality, contaminant-free, organic CBG enriched hemp products. Our vision is to become a global distributor of organic CBG infused products that will provided medical and therapeutically benefits to the end user.
Company Size (Fulltime employees)
Year of foundation
2014
Stock Market and Ticker/Symbol/Number
MGWFF
Please specify your partnering goal
END PRODUCT TO CHINA
Funding Status
1ST TRANCHE
Now raising (In USD)
1 MILLION
Headquartner in China
Plan in China
Strategic development into extracting and manufacturing CBG isolate and oil medical, health supplement and cosmetics with our own brand name to China and Asia market
Biotech/Pharma Category
TED FUNG
International Sales Manager 
Functionality

HebeCell Corporation United States

HebeCell was founded in 2016 by industry leading inventors in developing the manufacturing platform of hematopoietic cells from human pluripotent stem cells (PSCs). Their first-in-class proprietary 3D manufacturing platform for human iPS-NK cells is feeder-free, designed specifically for single-use-bioreactor at industrial scale. HebeCell’s platform will accelerate the application of PSCs as a viable source of immune cells in the next generation of immune cell therapies for immune-Oncology, autoimmune and infectious diseases.

Dr. John Lu is the President and CEO of HebeCell. Before establishing HebeCell, John was the Senior Director of Research at Advanced Cell Technology/Ocata Therapeutics, which in 2016 was acquired by Astellas, the second-largest pharmaceutical company in Japan. John is an expert in stem cell biology and regenerative medicine with 20 years of experience in the field.

Dr. Allen Feng is the Chief Scientific Officer of the HebeCell Corp. Prior to establishing HebeCell, he was the Director of Cell Biology of Semma Therapeutics, which was acquired by Vertex Pharmaceuticals in 2019. Prior to Semma, Allen worked as R&D Head of Stem Cell Bioprocessing Group at EMD Millipore, and also served as Director and Senior Scientist at Advanced Cell Technology /Ocata Therapeutics.
Company Size (Fulltime employees)
Year of foundation
2016
Please specify your partnering goal
Looking for Big Biotech/Biopharm to form strategic partnership, co-develop our proprietary PSC-CAR-NK platform and move into clinics
Funding Status
Series A
Now raising (In USD)
30 to 50 million USA
Headquartner in China
Plan in China
Joint Venture
Biotech/Pharma Category
John Lu
President and CEO 
Functionality

Helsinn Pharmaceuticals China Switzerland

Helsinn is a privately-owned Swiss Pharma Company which, since 1976, has been improving the lives of patients, guided by core family values of respect, integrity and quality. The Group has an extensive portfolio of marketed innovative cancer and rare disease therapies, a robust drug development pipeline and ambitions to further accelerate its growth through in-licensing and acquisition to address unmet medical needs. Helsinn operates a unique integrated licensing business model, achieving success with over 80 long-standing partners in 190 countries, who share our values. The Group’s pharmaceutical business, (Helsinn Healthcare) is headquartered in Lugano, Switzerland with operating subsidiaries in the U.S. (Helsinn Therapeutics US) and China (Helsinn Pharmaceuticals China) which market the Group’s products directly in these countries. The Group has additional operating subsidiaries in Switzerland (Helsinn Advanced Synthesis, an active pharmaceutical ingredient manufacturer) and Ireland (Helsinn Birex Pharmaceuticals, a drug product manufacturer). Helsinn Investment Fund was created to enhance the future of healthcare by providing funding and strategic support to innovative companies.
Website:
www.helsinn.com
Please specify your partnering goal
Out-licensing and exploring development/commercial partnerships in China
Headquartner in China
Enrico Magnani
General Manager 
Functionality

HungaroTrial CRO Hungary

When your clinical trial has to Overachieve in Central and Eastern Europe, HungaroTrial is here to help. Providing services for Phase 1 through Phase 4 clinical trials in Hungary, Czech Republic, Slovakia, Romania, Serbia, Croatia, Bulgaria, Bosnia, Poland, Ukraine, Belgium and Russia, HungaroTrial is the CEE region’s leading independent CRO.

To Overachieve, your clinical trial needs the best minds from beginning to end. That’s why Hungarotrial’s full-time staff includes 12 MDs of various specialties,more than any other independent CRO in the region. And you can be assured that our experienced team has built strong relationships with the most respected Key Opinion Leaders in CEE.

Our staff’s broad medical experience means that your clinical study benefits from diverse skills and synergistic teamwork. Over the past 18 years, HungaroTrial has become well known not just for this broad expertise, but also for our deep experience in Oncology, Rheumatology, Cardiovascular diseases, PAO, CNS and some other focus therapeutic areas.
Company Size (Fulltime employees)
Year of foundation
2000
Please specify your partnering goal
Clinical Services
Headquartner in China
Your Service Name
CRO
Service Description
Clinical services
Target Client Type
Biotech - Pharmaceuticals - Medical Device
Matteo Manco
Matteo Manco
LinkedIn logo BDD 
Functionality

i3 Consult France

We are an information-based consulting, integration and IT outsourcing service entity committed to providing premium strategic marketing, financial and operational management solutions for healthcare, pharmaceutical and other life science organisations.
Company Size (Fulltime employees)
Year of foundation
2002
Funding Status
Non-funding status - Profit based organisation
Headquartner in China
Plan in China
The defining characteristic of COVID era pharma and healthcare is the rise of all things digital. A critical mass of companies had been experimenting with digital pilots for some time, some more advanced and larger than others. All saw a significant boost in digital activities during the COVID-19 crisis. This included large scale webinars to engage Key Opinion Leaders (KOLs), disease education programs on a scale not seen before, all-digital new medicine launches, etc. Digital has arrived and is here to stay. Yet, offline has not yet disappeared and will continue to play an essential role. The real answer going forward will be found in the ability of i3 Consult to implement customer engagement hybrid models that build on offline and online activities to offer a true omnichannel engagement model to clients in China. We see the need to develop these opportunities in six (6) niche areas in China: 1) To strengthen retail KA management with distributors and pharmacies in China 2) Enhance commercial capabilities on broad market and retail channel 3) Better patient education to lead trend of prescription outflow from hospitals and retail channels 4) Provide HCP consultation support onsite for professional medical service 5) Improve drug availability through better collaboration and coverage with pharmacies in China 6) Enhance supply chain support by adding cold-chain capability and lower tier market coverage in China
Wallace Macindoe
CEO & Founder 

ImmunoBiochem Canada

ImmunoBiochem has pioneered a proprietary technology to address the challenges of cancer heterogeneity and tumor penetration by biologics in solid tumors with its tumor microenvironment-targeted potentiated antibodies. ImmunoBiochem's biologics are aimed at targets amplified in the secretomes of cancer cells that enable selective and efficacious delivery of payloads in tumor cells, immune cells and tumor-supporting stroma within the tumor microenvironment. ImmunoBiochem is able to deliver novel immunomodulatory payloads to a variety of cell types within the tumor in a highly selective fashion, pioneering a next-generation strategy for the delivery of innate immune system modulators.
Funding Status
Seed
Headquartner in China
Plan in China
Partnering for co-development and out-licensing. Open to collaborations, investment, JVs, partnering and out-licensing.
Anton Neschadim
Director 
Functionality

Incuron, Inc. United States

Incuron is a private clinical-stage company that develops a novel class of synthetic small molecules, Curaxins, with a unique multi-targeted mechanism of antitumor activity. These chromatin damaging agents interfere with histone/DNA binding causing decondensation of chromatin in tumor cells, functional inactivation of histone chaperone FACT, and simultaneous effect on a set of universal previously undruggable targets, leading to inhibition of pro-cancer transcriptional factors, MYC, NF-kB, HIF1a, and HSF-1, and activation of the tumor suppressor p53, as well as induction of type I interferon response.
Key advantages of curaxins based on current preclinical and early clinical data include:
- novel mechanism of action that would bring the additional treatment option for advanced and relapsed tumors, as well as potential to overcome resistance to previous treatments;
- favorable pharmacology and manageable safety profiles;
- low potential for serious drug-drug interactions providing opportunities for combinatorial therapeutic regimens;
- broad activity in different tumor types that may open wider market opportunities;
- focused phase 2 clinical study program can establish faster clinical proof of concept and build toward accelerated regulatory approval.
Incuron owns a worldwide patent portfolio, including the composition of matter and therapeutic uses of the compounds.
Website:
incuron.com
Headquartner in China
Plan in China
Incuron is currently seeking investors and partners for co-development to execute Phase 2 clinical program or out-licensing opportunities.
Kristina Zakurdaeva
CEO 
Functionality

iNNOGING Medical Israel

iNNOGING Medical - Remote and offline ultrasound image analysis solution

Ultrasound is a real-time examination and very much operator dependent.
Majority of ultrasound scans are done by technicians and afterwards diagnosed off-line by the expert without the presence of the patient. A major drawback is that the radiologist who determines the diagnoses is not the person who performs the ultrasound scan; hence this workflow might lead to errors and worse to misdiagnoses.
iNNOGING is developing a technology that will provide the radiologists a remote and off-line tool to inspect areas of interest, based on recorded ultrasound scans. Allowing navigation like in real time as if the patient is there with the doctor, while all possible information (any plane) of an organ is visible, even information that was not presented in the original scan.

In addition to the above, we have recently launched an affordable SaaS based Ultrasound Simulator.
Website:
www.innoging.com
Company Size (Fulltime employees)
Year of foundation
2018
Looking for
Funding Status
Seed round done, going to A-Round now
Headquartner in China
Plan in China
We would like to do one of our first clinical trials in China. to aqcuire a CFDA. The Chinese market is growing tremendously and we think it should be the main target for us.
Yehiel Polatov
Co-Founder EVP Business Development 
Functionality