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Selvita to acquire Fidelta from Galapagos

Galapagos NV [Euronext & NASDAQ: GLPG] and Selvita S.A. [WSE: SLV] – announced today that they have signed an agreement under which Selvita will acquire 100% of the outstanding shares in Fidelta d.o.o. for an enterprise value of € 31.2M plus the customary adjustments for net cash and working capital.

Fidelta is a contract research organization within the Galapagos Group of companies, with core scientific competences in inflammation, fibrosis, and anti-infectives. It currently employs 181 employees, including over 150 highly experienced scientists, providing integrated drug discovery services in the biotech and pharmaceutical industry, with a proven track record of accomplished laboratory projects over many years. Fidelta is located in state-of-the art R&D facilities in Zagreb, Croatia which offer almost 6,000 m2 of research space. The transaction is subject to customary closing conditions and is expected to close on the 4th of January 2021.

Galapagos is a fully integrated biopharmaceutical company with a deep pipeline of novel mechanism of action candidates and commercial operations in Europe; as such, the CRO activities offered by Fidelta no longer fit with its strategy.

Upon completion of the acquisition, Fidelta will be fully consolidated under the Selvita Group, and will continue to operate under the Fidelta name.

The scope of services provided by Fidelta is complementary to Selvita’s offerings and will enable Selvita to build a competitive advantage in business areas such as DMPK, in vivo pharmacology, and toxicology. Selvita will also increase its scale of operations within medicinal chemistry and in vitro pharmacology, resulting in significant strengthening of its market position.

Fidelta’s therapeutic areas of expertise align with current market trends, as infectious diseases, inflammation, and fibrosis are all areas of core expertise for Fidelta and are becoming increasingly major areas of interest for pharma companies due to the significant and unmet medical needs.

“We are thrilled to announce our acquisition of Fidelta. This is a perfect fit for us: an extensively experienced organization, with a full range of in-house drug discovery capabilities and an established track record of clinical candidate delivery,” says Boguslaw Sieczkowski, Chief Executive Officer at Selvita. “With this acquisition, we are not only executing our strategy announced this year, but we’re actually taking a leap in both the scope of our services portfolio and the scale of business. It is a transformative moment in the history of Selvita.”

“The scientific knowledge, the business acumen, and the focus and commitment of the team at Fidelta are second to none.  I would like to thank the Fidelta team for the excellent collaboration over the years.  I’m sure they will thrive under the Selvita umbrella. We will continue part of our discovery work with Fidelta, so we will benefit from that,” says Onno van de Stolpe, CEO of Galapagos.

“We are very happy to take this big and logical step in the further development of Fidelta, and together with Selvita, to strengthen our presence on the market. Bringing together these two companies will allow us to keep a high level of quality and offer an even more integrated approach  in services that we provide to our clients,” says Adrijana Vinter, Managing Director of Fidelta.

Source: Galapagos (Press release)

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Leestip FD: Oproep voor een gunstiger startupklimaat

Stimuleer startups met een aantrekkelijk financieel klimaat is de oproep van o.m. Alexander Rinnooy kan, Jeroen van der Veer en Prins Constantijn in het Financieele Dagblad vorige week. Daartoe doen zij drie verschillende aanbevelingen.

  1. Maak medewerkersparticipatie mogelijk
  2. Stimuleer herinvesteringen naar het voorbeeld van Sillicon Valley
  3. Stel een impactkorting in

De briefschrijvers richten zich met name op tech startups, maar HollandBIO vindt dat de voorgestelde maatregelen juist ook toepasbaar zijn op kennis- en kapitaalintensieve biotech startups. Op die manier kan Nederland alle vruchten plukken van al het moois dat onze sector te bieden heeft.

Lees het hele bericht hier: https://fd.nl/opinie/1363931/een-goed-klimaat-voor-startups-vraagt-fiscale-aanpassingen

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CureVac and WACKER Sign Manufacturing Contract forCureVac’s COVID-19 Vaccine Candidate:CVnCoV

CureVac N.V. (Nasdaq: CVAC), a biopharmaceutical company developing a new class of transformative medicines based onmessenger ribonucleic acid (mRNA), and Wacker Chemie AG announced today that they had signed a contract for the manufacturing of CureVac’s COVID-19 vaccine candidate CVnCoV. Under the terms of the initial agreement, WACKER will ramp up GMP (Good Manufacturing Practice) production of the mRNA drug substance for CVnCoV at its biotech site in Amsterdam in the first half of 2021.Preparationsfor the start of production, technology transfers and test runs are already underway.It is planned to produce more than 100 million doses of the CureVac vaccine per year at WACKER’sAmsterdam site.There is also further potential for expansion at the site in order to meet rising demand in the future.

WACKER’s CEO Rudolf Staudigl said: “We are proud and highly motivated to make a contribution to the fight against the spread of the coronavirus pandemic together with CureVac.” As a CDMO (Contract Development and Manufacturing Organization), Wacker Biotech bundles WACKER Group’s biopharmaceutical activities. Its Amsterdam site has been producing vaccines for clinical development and commercial supply for 20 years. The portfolio ranges from conventionallive and killed vaccines to protein-based, polysaccharide and glycoconjugate vaccines. In recent months, WACKER has invested in the site to extend production to includemRNA-based vaccines. This new classof vaccines expands the broad vaccine portfolio Wacker Biotech offers to its customers.

Dr. Florian von der Mülbe, Chief Production Officer of CureVac, added:“With WACKER, we have found a committed and highly experienced partner for the production of our vaccine candidate in the Netherlands.”CureVac is building an integrated European vaccine manufacturing network with several CDMO partners. With this strategy, the company will significantly increase the manufacturing capacity already existing within CureVac for CVnCoV up to several hundred million doses per year and will manage potential supply chain risks by working with several partners for each of the key manufacturing process steps.

Source: Wacker (Press release)

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Pharvaris Announces $80 Million Series C Financing to Advance Novel Oral Bradykinin-B2-Receptor Antagonists for the Treatment of HAE

Pharvaris, a clinical-stage company focused on the discovery and development of novel oral bradykinin-B2-receptor antagonists for the treatment of hereditary angioedema (HAE) and other bradykinin-B2-receptor-mediated indications, announced the close of its oversubscribed $80 million Series C financing bringing its total venture funding to over $160 million to date. Viking Global Investors and General Atlantic co-led the financing, with participation by Cormorant Asset Management. Current investors Foresite Capital, Bain Capital Life Sciences, venBio Partners, and Venrock Healthcare Capital Partners also participated in the round.

“Our team is committed to developing and delivering differentiated products to patients – the oversubscription of our Series C highlights broad enthusiasm for our vision for HAE and beyond,” said Berndt Modig, Chief Executive Officer and co-founder of Pharvaris. “The backing from this prominent group of investors will enable us to develop our pipeline of compounds for the treatment of HAE and other bradykinin-B2-receptor-mediated indications. We expect to complete our Phase 1 assessments in healthy volunteers at the end of the year and anticipate announcing top-line data in 2021.”

The proceeds from the Series C financing will fund the clinical advancement of Pharvaris’ pipeline of novel oral bradykinin-B2-receptor antagonists for the treatment of HAE, including both on-demand treatment and prophylactic prevention. Pharvaris’ first product candidate, PHVS416 (PHA121 in soft capsules), is a potent, orally available bradykinin B2-receptor antagonist designed to block the effects of bradykinin during HAE attacks. Initiation of RAPIDe-1, a multi-center Phase 2 placebo-controlled on-demand study of PHVS416 in HAE patients, is expected in 2021. Pharvaris is also developing an orally available extended-release product containing PHA121 specifically for prophylaxis in HAE patients.

Brett Zbar, M.D., Managing Director and Global Head of General Atlantic’s Life Sciences sector, stated, “As I saw during my previous tenure as a director, Pharvaris has a demonstrated track record of executing against its development strategy for PHA121, underscored by the promising clinical data presented at ACAAI last week. We strongly believe in Pharvaris’ mission and are excited to back Berndt and the team as we put further momentum behind General Atlantic’s Life Sciences strategy.”

Source: Pharvaris & LSP

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Pharming gaat nieuwe downstream-productiefaciliteit voor RUCONEST® bouwen op Pivot Park in Oss

Pharming Group N.V. (Euronext Amsterdam: PHARM) maakt bekend dat het zich heeft gecommitteerd tot het bouwen van een nieuwe productiefaciliteit ter uitbreiding van de verwerkingscapaciteit van het hoofdproduct RUCONEST® (recombinant C1-esteraseremmer (rhC1INH)).

De zogeheten downstream-productie omvat de zuivering, filtratie en concentratie van het startmateriaal. De bouw start medio 2021 op het Pivot Park in Oss. Pivot Park is ook de locatie van BioConnection B.V., de fill & finish-partner van Pharming, waarin een minderheidsbelang wordt gehouden.

Op Pivot Park betrekt Pharming een nieuw, duurzaam gebouw van vijf bouwlagen met een totale vloeroppervlakte van circa 4.000 m². Het gebouw is specifiek voor Pharming ontworpen en is prominent gesitueerd op het terrein. Het is het eerste nieuwe gebouw op de campus en CEO Drees hoopt dat er nog veel meer zullen volgen. De komst van Pharming naar Pivot Park zorgt voor tenminste zo’n veertig nieuwe arbeidsplaatsen in Oss.

Sijmen de Vries, Chief Executive Officer van Pharming, zegt: “Met een groeiende vraag naar RUCONEST® voor de behandeling van erfelijk angio-oedeem en een toenemende behoefte aan rhC1INH voor onze klinische onderzoeken bij nieuwe, grote indicaties, blijven we investeren in de uitbreiding van onze interne verwerkingscapaciteit als onderdeel van onze lange-termijn groeistrategie. We kijken uit naar de start van bouw van de nieuwe fabriek medio 2021.”

Brigitte Drees, directeur van Pivot Park, zegt: “Pharming is een aanwinst voor onze campus. Enerzijds omdat het bedrijf een gevestigde naam is in de farmaceutische industrie. Anderzijds omdat het openstaat voor open innovatie en kennisdeling, net als de ruim zestig bedrijven die hier al gevestigd zijn. Reken maar dat Pharming zich in onze community snel thuis zal voelen. Én dat we het bedrijf goed zullen faciliteren in zijn ontwikkeling.”

Source: Pharming Group & Pivot Park

Read more: Brabants Dagblad

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Immunicum AB and DCprime Combine Forces to Establish Leader in Cell-Based Cancer Immunotherapies

Immunicum AB (publ) (IMMU.ST) announced that it has entered into an agreement with Van Herk Investments B.V. to acquire all of the shares in DCprime B.V., a Dutch clinical stage company developing cancer relapse vaccines aimed to reduce tumor recurrence (the “Transaction”). Merging the complementary allogeneic dendritic cell biology approaches of both companies will enable Immunicum to further build and strengthen its position as a leader in cell-based cancer immunotherapies. Payment in the Transaction is effectuated through an issue in kind of 73,909,635 new shares in Immunicum representing 44 percent of the shares in Immunicum on a fully diluted basis. DCprime’s current majority shareholder, Van Herk Investments B.V., a leading European life science investor, will thereby become a significant shareholder of the combined entity. The issuance of the shares is subject to approval by an Extraordinary General Meeting (EGM) to be held on December 18th, 2020.

The main objective of the combination is to establish a unified company built on decades of combined immuno-oncology and cell therapy expertise in the field of allogeneic dendritic cell biology. Moving forward, Immunicum’s scientific focus will continue to be on triggering immune responses against established tumors via intratumoral immune priming and expanded to include the reduction of tumor recurrence via relapse vaccination. To date Immunicum has established clinical proof of concept for its lead program, ilixadencel, which has been tested in a range of solid tumors. DCprime has produced equally encouraging clinical results for blood-borne tumors including interim data from its ongoing Phase II study in Acute Myeloid Leukemia (AML), which will be provided in an oral presentation at the upcoming ASH 2020 conference. Together, the companies will advance a synergistic pipeline spanning both large and orphan indications in solid as well as blood-borne tumors, with two programs in Phase II clinical development and multiple near-term value inflection points as well as a portfolio of preclinical programs and research capabilities to fuel future pipeline expansion. Importantly, the combined process development and manufacturing expertise and specialized in-house research and development facilities will support the shared goal of becoming a leader in the development of cell-based immunotherapies.

The newly combined company will maintain its corporate headquarters in Stockholm, Sweden and consolidate research, process development and future manufacturing efforts at the location in Leiden, the Netherlands. Immunicum’s shares will continue to trade on the Nasdaq Stockholm.

Following the closing of the transaction, Erik Manting, Ph.D., currently CEO of DCprime, will join Immunicum’s leadership team as Chief Business Officer and deputy CEO. Jeroen Rovers, MD, Ph.D., currently Chief Medical Officer at DCprime, will have the role of the Managing Director of DCprime in the combination. Erik Manting brings several years of research experience in immunology as well as 15 years in commercial and management roles in banking. Jeroen Rovers brings 15 years of industry experience in a variety of medical roles, including CMO at Kiadis Pharma.

In addition, Immunicum will call for an EGM in order for the shareholders to resolve upon the proposed elections of Andrea van Elsas, Ph.D. and Dharminder Chahal to the Board of Directors of Immunicum. Andrea van Elsas is currently a venture partner at Third Rock Ventures, and his scientific career includes leading the anti-PD1 program that became leading immunotherapy, pembrolizumab (Keytruda®). Dharminder Chahal is CEO and co-founder of an oncology diagnostics company, SkylineDx, and investment manager to Van Herk. Van Herk is a leading European investor in life science having made a number of successful investments including Zealand Pharma, Ablynx, Crucell and Galapagos. Van Herk is also the largest shareholder in Swedish listed biotech company, BioInvent, where Dharminder Chahal serves as a board member.

By way of the Transaction, Immunicum will acquire all outstanding shares in DCprime. Payment in the Transaction is effectuated through an issue in kind of 73,909,635 new shares in Immunicum to Van Herk. The share purchase agreement has been entered into with Van Herk Investment B.V. and has been adhered to by Van Herk Royalty B.V., which is a company within the Van Herk Group and the current shareholder of the shares in DCprime. Before closing the shares will be transferred to Van Herk Investments B.V. Further, prior to the closing of the Transaction, Van Herk will acquire the minority shareholders’ shares in DCprime and such minority shareholders will consequently partly be paid in cash and partly in Immunicum shares. As a result of the Transaction, Van Herk will be the largest shareholder in Immunicum, holding approximately 43 percent of the total outstanding shares after the Transaction. Customary lock-up provisions covering a period of twelve months have been put in place between Immunicum, Van Herk and DCprime minority shareholders receiving issued shares.

Van Herk Investments, together with Immunicum’s largest shareholder, Fourth Swedish National Pension Fund (AP4), have expressed their support to the new, combined entity. In addition, Van Herk Investments, Immunicum’s largest shareholder following the Transaction, intends to invest up to SEK 82.5 million in the company.

Closing of the Transaction is conditional upon approval of issuance of the shares by the EGM, with a two-thirds majority requirement for the approval of both the votes cast and the shares represented at the EGM,1 approval and publication of the prospectus, and Van Herk’s acquisition of the minority shareholders’ shares in DCprime. The closing of the Transaction is expected to take place at the end of December 2020.

Immunicum’s assessment is that the current funds available for the combined entity will be sufficient to finance operations into the beginning of 2022 based on immediate financial benefit from the companies’ operational synergies. Immunicum will further propose to the EGM the approval of a mandate for the Board of Directors to resolve to issue shares in a directed issue of up to 20 percent of the outstanding shares after the Transaction to facilitate financing activities.

“As announced in the recent corporate and clinical update from September, one of Immunicum’s main goals is to expand the Company’s pipeline with the vision of becoming a leading cell therapy company. As such, joining forces with DCprime, an innovative company with extensive  expertise in allogeneic dendritic cell biology, stands as an exciting opportunity with great potential for Immunicum that will build additional value for the Company, our shareholders and future patients,” stated Sven Rohmann, MD, Ph.D., Chief Executive Officer of Immunicum. “Together, we can pursue the treatment of both solid tumor and blood-borne tumors by intratumoral priming as well as systemic boosting using the next-generation of allogeneic, off-the-shelf cell-based therapies. Our teams and our technologies are complementary and would significantly increase the potential of our pipeline and deliver more value-inflection points and potential partnering opportunities.”

“DCprime has established a strong position in cell-based cancer therapy with a Phase II asset in blood-borne tumors. By integrating with the Immunicum team, we look forward to the continued advancement of our unique relapse vaccine approach in parallel to the ongoing clinical progress of Immunicum’s lead candidate, ilixadencel,” stated Erik Manting, Ph.D., Chief Executive Officer of DCprime. “From a corporate perspective, DCprime’s and Immunicum’s lean and focused organizations and excellent teams are the perfect match to drive the development of the combined pipeline products and identify additional novel therapeutic solutions to address unmet medical needs in the field of cancer therapy.”

“This transaction is a transformative milestone for Immunicum as it will bring additional value to the company and enable it to further establish itself as a leader in the development of cell-based immuno-oncology treatments,” said Michael Oredsson, Chairman of the Board at Immunicum. “Together, we will have world class competence with in-house process development and manufacturing expertise and specialized research and development facilities as well as strengthened ownership by the addition of Van Herk, a renowned and committed life science investor known for their success stories in Galapagos and Zealand Pharma, BioInvent, Galapagos and successful trade sale exits in Ablynx (Sanofi), Crucell (J&J), among others.”

“The combination of Immunicum and DCprime creates a well-positioned company with a broad pipeline with two programs in the clinical phase as well as several preclinical opportunities,” said Dharminder Chahal, Chairman of the Board at DCprime and representative for Van Herk. “We look forward to supporting Immunicum as the company further advances its innovative immuno-oncology projects.”

Source: Immunicum (Press release)

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Catalyze to receive FD Gazelle 2020 award

Catalyze is thrilled to announce that we have been selected once again to receive the prestigious FD Gazelle 2020 award. The FD Gazellen is awarded by Het Financieele Dagblad to companies that meet certain selected criteria, in recognition of their rapid, successful growth. Being elected a FD Gazelle 2020, Catalyze is recognized as one of the fastest growing companies in the Netherlands.

Catalyze is proud to receive this award, as it signifies our increasing capacity to supply our unique blend of services to our academic and business partners in the life sciences, but also in agriculture, food and bioeconomy. At Catalyze we push hard and are fully dedicated to support the latest groundbreaking scientific innovations. With our continued growth, we are able to contribute to the success of an ever-increasing number of impactful projects. For this, we thank all of our fantastic partners, clients and most importantly, our colleagues. 

“This is a great recognition for our company. Our client base continues to grow and as Catalyze we continue to expand our service offering and expertise to better serve their needs. I am very thankful to our ambitious team that works hard every day to make a difference. This is a great acknowledgement.” – Theodoor Rutgers, founder and director.

As an organization, we look forward to continuing this exciting journey being at the forefront of our field, where we make a real difference and together, make positive and sustainable impact!

Source: Catalyze (Press release)

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Lead Pharma uit Oss sluit deal voor €260 miljoen met Roche

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Lead Pharma, een farmaceutische onderneming die innovatieve geneesmiddelen ontwerpt en ontwikkelt voor de behandeling van auto-immuunziekten en kanker, maakt bekend dat het een samenwerkings- en licentieovereenkomst heeft gesloten met Roche voor de ontwikkeling van een nieuwe klasse van kandidaat-medicijnen voor de behandeling van een breed scala aan immunologische aandoeningen.

Lead Pharma en Roche werken samen aan een nieuwe klasse van medicijnen met een nieuw werkingsmechanisme. De samenwerking moet leiden tot een kandidaat-medicijn, waarna Roche verantwoordelijk zal zijn voor de verdere (klinische) ontwikkeling en wereldwijde commercialisering.

Conform de overeenkomst ontvangt Lead Pharma na tekenen een betaling van € 10 miljoen en komt het in aanmerking voor onderzoeks-financiering. Lead Pharma kan in de toekomst betalingen ontvangen die gekoppeld zijn aan het behalen van een aantal specifieke onderzoeks- en ontwikkelingsresultaten.

De totale betalingen kunnen oplopen tot € 260 miljoen, plus royalty’s op de wereldwijde verkoop van de te ontwikkelen medicijnen.

“Onze ambitie is om levensveranderende behandelingen voor patiënten te ontwikkelen. We zijn zeer verheugd over de samenwerking met Roche om dit doel gezamenlijk te kunnen realiseren ”, zegt Frans van den Berg, Chief Executive Officer van Lead Pharma. “Samenwerking met farmaceutische partijen vormt een van de pijlers van onze strategie, en deze samenwerking onderstreept de toegevoegde waarde van Lead Pharma’s innovatiekracht.”

Arthur Oubrie, Chief Scientific Officer van Lead Pharma, vult aan: “Dit is het tweede project waarin we met een van de grootste mondiale farmaceutische bedrijven samenwerken. De manier waarop wij nieuwe projecten selecteren, de werking van medicinale stoffen onderzoeken in farmacologische modellen, en onze hoogstaande medicinale chemie, waren essentieel bij de ontwikkeling van dit project tot aan dit stadium. We kijken uit naar de samenwerking met de specialisten bij Roche om deze nieuwe therapie zo snel mogelijk naar de patiënt te brengen.”

“We are committed to advancing innovative science and transformative medicines for people affected by different immune mediated diseases”,  zegt James Sabry, Global Head, Roche Pharma Partnering. “We are looking forward to further building on our expertise in this field and collaborating with Lead Pharma, aiming to make a difference for those patients.”

Bron: Lead Pharma (Persbericht)

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New fund to impact tomorrow’s healthcare: launch of Thuja Capital Healthcare Fund III

Thuja Capital Management (Thuja) announced completion of a first closing of its third investment fund, Thuja Capital Healthcare Fund III (TCHF III). TCHF III will invest in early-stage innovative companies and daring entrepreneurs developing best-in-class products with clinically proven benefits for patients to impact the healthcare of tomorrow.

The products of the companies Thuja invests in are deeply rooted in science and clinical practice. In close collaboration with universities and university medical centers (in particular those of Utrecht, Maastricht (Brightlands), Nijmegen and Leuven) Thuja will be scouting for projects to build new ventures focusing on novel therapeutics, medical devices, nutraceuticals or digital health solutions with high impact potential. In addition, Thuja is deeply involved with important innovation ecosystems through its relationship with a number of regional development agencies and investment funds (BOM, Oost NL, LIOF, NOSHAQ and Sambrinvest).

Oscar Schoots, Utrecht Holdings (representing both Utrecht University as well as Utrecht University Medical Center): “We are participating in a Thuja fund for the third time in a row now. Over the past decade we have found a valuable investor and partner in Thuja, committed to providing not only the financial resources but also broader strategic and practical support to get our spin-off companies going and facilitate their way to success.”

Over the next years, Thuja will invest in 10 to 15 companies mainly in The Netherlands, Belgium and Germany. Thuja’s relationship with NOSHAQ, Sambrinvest and KU Leuven further cements Thuja’s engagement in the innovation-rich Belgian ecosystem.

Initial capital providers to TCHF III include the European Investment Fund (EIF), under the Innovfin mandate.

Alain Godard, Chief Executive of the EIF: “Thuja has been performing very well since we joined as a cornerstone investor in their second fund. We recognize their role in nurturing a vibrant innovation ecosystem and value their relationships with universities to create and nurture novel companies. Our decision to join Thuja’s third fund also shows the importance of the support from European institutions to boost innovation around Europe.”

In addition to EIF, mentioned universities and regional development agencies also committed to TCHF III, supplemented with a number of family offices and private individuals. At this time, the fund has a starting capital of EUR 43M but expects to raise EUR 75M to EUR 100M once fully completed.

With the first closing of TCHF III completed, Thuja is expanding its team. Aartie Nanda has recently joined Thuja as an office and communications manager, and further hires to reinforce the investment team are in progress.

As an investor in healthcare companies, Thuja aims to positively impact the lives of patients and promote health. In order to optimize the impact potential of portfolio investments, Thuja will implement ESG factors alongside financial risk management. Thuja has appointed an Impact and ESG officer to the team to support this ambition.

Source: Thuja Capital (Press release)

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Grenoble Ecole de Management offers free-of-charge marketing & technology studies

Grenoble Ecole de Management proposes to offer free of charges the services of our students to work on a marketing and technology study. Grenoble Ecole de Management is a French business school with an international advanced master in biotech and pharma management (fully in English). This advanced master trains students with a strong scientific background, how to work at the interface between technologies and business. It is recognised to be the best advanced master of pharmaceutical marketing & management in France.

Between December and May, our students will work in small groups (2-4) on a concrete innovative project. They will be tutored by one of our teachers. The projects should include 3 parts:

  • Evaluation of the technologies at play in a particular industry or sector
  • Complete market analysis for that industry or sector (market size, growth rate, competitor analysis, channels, market trends…)
  • Additional questions of your choosing tied to strategy, finance, competitive intelligence, marketing…

It is an occasion for you to propose a project free of charges but also to know our students and our master.

As a list of projects will be sent to our students on the 6th of December, we would ask you to send us a draft of the project before the 28th of November to have enough time to adjust together the project to the requirements of the master.

For this project, we would request from your company:

  • A 4-8 PowerPoint slide presentation in English that explains what your company does and what your technology is (a short corporate presentation also works well)
    • The document needs to include specific questions that you would like the students to work on. (They will automatically prepare a technological comparison and a market analysis).
    • We can help you writing the questions so that there are no misunderstandings about the deliverables
    • It also needs to include the contact information of the persons that will interact with the students
  • Be available to answer questions about your company, or about the industry that you’re working in.
  • Give some sort of basic feedback about what you thought of the work the students did for you.

We can send you examples of questions asked to the students last year.

Contact information: samuel.collaudin-external@grenoble-em.com