Portal for life science/healthcare startups
  • Home
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    • 日本語トップ
  • Table of Contents (English)
    • Business Setup & Operations >
      • Startup Visa
      • setup corporation, office in Japan
      • Company establishment
      • Life Science Hub, Startup Hub
    • Regulatory & Compliance >
      • PMDA consultation
      • regulatory considerations when using person infformation
      • Guide to Selecting Regulatory Affairs Staff and Consultants
      • Expedited Review Systems for Pharmaceuticals
      • Guidelines for Establishing Generic Drug Names
      • Combination Products, Combination Medical Devices, Kit Products, Combination Drugs
    • Medical Device, IVD >
      • IVD, LDT, RUO
      • DMAH: Designated Marketing Authorization Holder-Summary Ver.
      • Combination Products, Combination Medical Devices, Kit Products, Kit Components, Assortment Products
      • How to determine if a product is a medical device
      • medical device classification for combined products
      • Classification of Medical Devices
      • how to confirm JMDN of medical device
      • medical device & IVD reimbursement-Summary Ver.
      • medical device & IVD reimbursemenet
      • insurance reimbursement for SaMD
      • Comparison of Medical Device Definitions: Japan, US, & EU
      • Companion Diagnostics and Gene Panel Testing
    • Pharmaceutical, regenerative medicine >
      • How to determine if a product is a Pharmaceutical Drug
      • Advanced Medical Care System
      • Over-The-Counter (OTC) Drug
      • References on Reimbursement (Cost Calculation) for Regenerative Medical Products
    • Healthcare & Caretech Products >
      • guidance for non medical services
      • Therapeutic Orthoses and Assistive Devices
      • Cosmetics and Quasi-Drugs
      • Overseas Expansion of Non-Medical Device Products as Medical Devices: Learning from the Case of PARO
    • Funding, Partnering & Networking >
      • Utilization of Public Grants and Subsidies
      • J-Ships
    • Intellectual Property >
      • patent or trade secret?
      • employee invention
      • Matching of Patents Held by Startups and Individuals
    • Legal & Contracts >
      • References for Contracts
      • Guide to Industry-Academia Collaboration Agreements for Academic Researchers
    • Academia & Tech Transfer
    • Licensing, partnering >
      • Networking, Partnering
      • Introducing Seeds to Pharmaceutical Companies
      • Incentives (Returns) to Licensor Universities
    • References in English
  • コンテンツ一覧
    • 起業、法人設立・運営 >
      • 事業計画の策定
      • 法人設立
      • ライフサイエンスハブ、スタートアップハブ
    • 公的支援 >
      • 公的支援機関リスト
      • 大学発スタートアップ支援機関・プログラムガイド
      • AMED Medical IP Desk
      • MEDISO活用のススメ
    • 薬事・規制関連 >
      • PMDA RS相談活用のススメ
      • 薬事スタッフ・コンサル選定ガイド
      • 都道府県薬務課一覧
      • コンビネーション製品、組合せ医療機器、キット製品、組合せ医薬品
    • 医薬品、再生医療等製品 >
      • 医薬品の該当性確認方法
      • 医薬品一般的名称設定のガイドライン
      • 医薬品、医療機器等の開発に当たって、参照したい資料
      • 先進医療制度
      • 一般用医薬品(OTC)
      • コンパニオン診断薬と遺伝子パネル検査
      • 再生医療等製品の保険償還(原価計算)に関する参考情報
    • 医療機器、体外診断用医薬品 >
      • 体外診、ラボ開発検査、研究用試薬
      • 医療機器該当性確認ガイド
      • 医療機器と非医療機器の機能が複合した製品は?
      • 医療機器の一般的名称と確認方法
      • 医療機器のクラス分類
      • 医療機器・体外診の保険収載
      • SaMDの保険収載
    • ヘルスケア・ケアテック >
      • 非医療分野の検査サービスを展開する際に注意すべきポイント
      • 治療用装具と補装具
      • 化粧品及び医薬部外品
      • 医療機器とするか、非医療機器とするか
    • 資金調達 >
      • 公的な助成金、補助金の活用
      • 特定投資家向け銘柄制度(J-Ships)
      • アカデミア研究者がPIとして応募可能なグラントリスト
      • 海外在住の日本人研究者が日本の助成金を獲得する方法
    • 知的財産 >
      • 特許か?営業秘密か?
      • 職務発明:アカデミア・公的研究機関に所属する研究者が注意すべきポ
      • スタートアップや個人が保有する特許のマッチング
      • ライセンスを受けた大学へのインセンティブ(還元)について
    • 法務・契約 >
      • 契約関連で参考になる公的機関の資料
      • 個人情報を利用する製品開発時の 留意すべき法規制
    • アカデミア、技術移転 >
      • アカデミア研究者のための産学連携契約ガイド
    • ライセンシング、パートナリング >
      • 製薬企業等へのシーズ紹介
      • ネットワーキング、パートナリング
    • 海外展開 >
      • 米国展開(主に医療機器)に、読むと役立つ情報リスト
      • 米国FDAにおける、医療機器該当性の確認ステップ
      • 米国における、医療機器の申請データ・試験計画の相談方法((Pre-Submission/Q-Submission
      • 公的機関の海外展開支援
      • 横浜市の公的支援サービス
      • JETROを徹底活用しよう
      • 日米欧での医療機器定義の比較
      • 簡略審査(審査の迅速化)
      • 海外規制等の情報収集
      • 非医療機器製品の海外での医療機器展開
      • 欧州医療機器規則MDRに関する資料
      • 欧州MDRにおける、医療機器該当性の確認方法
    • オーストラリア >
      • オーストラリア研究開発優遇税制の概要
      • オーストラリア研究開発優遇税制の適用を受けるには
      • オーストラリアでの主要イベント
      • R&D関連の公的機関
      • オーストラリア助成金情報

Introducing Seeds to Pharmaceutical Companies

When startups pitch their products or technologies, the business development departments of pharmaceutical companies, etc., serve as the point of contact. Here, we will focus on the pharmaceutical industry.


  • Business Development Department
    • In the pharmaceutical industry, licensing operations are systematized, and most companies have dedicated departments and staff. This was originally a system adopted by global pharma, but domestic companies are now following suit.
    • Department names used to often be External Relations, Licensing, or Business Development, but recently, Open Innovation seems to be in vogue. Here, we will refer to them collectively as the Business Development Department.
    • Depending on the company, the department in charge may differ for early-phase and relatively late-stage items, but information is shared internally.
    • Some Japanese medical device manufacturers also have dedicated departments, but this is limited to major companies and they are not as well-staffed as those in pharmaceutical companies.
  • How to Find Needs
    • There are two main ways: one is the relevant webpages of individual companies, and the other is the needs information pages published by public organizations, etc. The main public organizations that post the needs of pharmaceutical companies are as follows.
      • JPMA (Japan Pharmaceutical Manufacturers Association)
        • Research and Development Needs of Committee Member Companies
        • https://www.jpma.or.jp/information/research/RD_needs/index.html
      • JBA (Japan Bioindustry Association)
        • Information on Research/Development Collaboration Opportunities from Companies
        • https://www.jba.or.jp/activity/open_innov/jbamember_directory/alliance/
      • AMED (Japan Agency for Medical Research and Development)
        • Seeds/Needs Matching Promotion Page
        • https://www.amed.go.jp/program/list/11/01/seeds-needs_list.html
    • Individual Companies
      • Please refer to each company's Open Innovation pages, etc. Also, most pharmaceutical companies have a needs list (called a wish list), so you can also inquire with the business development representative.
      • There are also private company websites that compile the needs of pharmaceutical manufacturers, so use them as needed.
      • If you belong to academia, the industry-academia collaboration department will be the contact point for external relations. They often already have the wish lists of pharmaceutical companies, and sometimes publish them on the university's website. Let's make active use of this.
  • Approach
    • Participate in networking events such as Bio Japan
      • The most efficient is Bio Japan.
        • https://jcd-expo.jp/jp/about.html
      • At that time, it is highly recommended to use the partnering system, although it is a paid service. By using this system, it becomes possible to set up meetings with many companies.
        • https://jcd-expo.jp/jp/partnering.html
    • Individual Approach
      • It is also possible to make inquiries through each company's website, etc.
  • Basic Flow
    • After confirming the other party's needs, contact their business development department through events like Bio Japan or by email.
    • First, you provide non-confidential materials for them to review.
    • The business development department reviews the content of the seeds to see if they fit with the priority development areas. Seeds that do not fit are rejected on the spot. If they do fit, they will check for interest with relevant internal departments.
    • If the other party is interested, there will be some inquiries, and usually a meeting request.
    • After the meeting, if they want to know more details, they will propose concluding a non-disclosure agreement (NDA).
    • After concluding the NDA and following several reviews, if there is a desire to partner, the pharmaceutical company will conduct due diligence (DD).
    • If the DD by the pharmaceutical company's internal and external DD specialist teams shows no particular problems, it will lead to a formal contract.
  • Common Questions/Misconceptions
    • "Isn't it better to pitch directly to the R&D department?"
      • Not highly recommended.
      • The areas targeted for licensing are closely linked to the company's management strategy. The business development department, which is the point of contact, is well-versed in this, but the R&D department is not necessarily so. Depending on the person, they might be involved in research that is outside the priority areas. In the first place, the business development people attending networking events like Bio Japan are approved by the company to participate, so introducing products and technologies through them is the proper approach.
      • "I'll talk about the details after signing an NDA."
      • In the case of pharmaceutical companies, they cull heavily at the non-confidential level (some companies reject about 70%). If you take the leisurely approach of "I'll talk about specifics after signing an NDA," you won't get to the next step. Of course, there is no need to include top-secret matters, but the materials must be thoroughly prepared.
    • "For global pharma, isn't it better to introduce it to the overseas headquarters?"
      • As a rule, the business development representative at the Japanese subsidiary will be the point of contact.
      • Most global pharma companies already have a Japanese subsidiary and Japanese business development staff.
      • In large companies, business development staff have assigned territories, and in most cases, seeds coming from Japan will be handled by the Japan business development team.
      • Similarly, seeds originating from Europe are handled by the European business development staff, and seeds from the US are handled by the US business development staff.
      • In any case, seed information is shared among the company's business development staff, so it's safe to say there is almost no difference depending on the point of contact.
    • "I was rejected once, but can I propose it again at another time?"
    • It's case-by-case, but if you were once clearly rejected as "not interested," the probability is low.
    • The response from a pharmaceutical company after providing non-confidential materials largely falls into the following three categories.
      • 1) We are interested, please explain it to us once.
      • 2) We are interested, but please contact us again after you've made more progress.
      • 3) We are not interested and will not conduct further evaluation.
    • 1 is literally a good response, and you will be given an opportunity for about an hour-long product/technology introduction, either online or in person.
    • In case 2, it matches their strategic area and they are interested, but due to reasons like insufficient POC, they want to evaluate it after more positive data is available.
    • 3 is a case where it is rejected because it doesn't match the strategic area in the first place, or the seeds are judged to be weak.
    • Therefore, if the response is 3, there is almost no chance. If it is 2, you can consider it possible to try again if you get good data.
    • When you start contacting companies, it is recommended to take individual notes of the companies' responses as described above, chronologically and for each company.
    • Also, be sure to take notes on feedback from companies. Even if it's negative feedback, scrutinize it and constantly improve your materials and activities.
    • This series of tasks is equally effective when contacting VCs for fundraising purposes.

©K.Kamitani
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  • Home
    • English Top
    • 日本語トップ
  • Table of Contents (English)
    • Business Setup & Operations >
      • Startup Visa
      • setup corporation, office in Japan
      • Company establishment
      • Life Science Hub, Startup Hub
    • Regulatory & Compliance >
      • PMDA consultation
      • regulatory considerations when using person infformation
      • Guide to Selecting Regulatory Affairs Staff and Consultants
      • Expedited Review Systems for Pharmaceuticals
      • Guidelines for Establishing Generic Drug Names
      • Combination Products, Combination Medical Devices, Kit Products, Combination Drugs
    • Medical Device, IVD >
      • IVD, LDT, RUO
      • DMAH: Designated Marketing Authorization Holder-Summary Ver.
      • Combination Products, Combination Medical Devices, Kit Products, Kit Components, Assortment Products
      • How to determine if a product is a medical device
      • medical device classification for combined products
      • Classification of Medical Devices
      • how to confirm JMDN of medical device
      • medical device & IVD reimbursement-Summary Ver.
      • medical device & IVD reimbursemenet
      • insurance reimbursement for SaMD
      • Comparison of Medical Device Definitions: Japan, US, & EU
      • Companion Diagnostics and Gene Panel Testing
    • Pharmaceutical, regenerative medicine >
      • How to determine if a product is a Pharmaceutical Drug
      • Advanced Medical Care System
      • Over-The-Counter (OTC) Drug
      • References on Reimbursement (Cost Calculation) for Regenerative Medical Products
    • Healthcare & Caretech Products >
      • guidance for non medical services
      • Therapeutic Orthoses and Assistive Devices
      • Cosmetics and Quasi-Drugs
      • Overseas Expansion of Non-Medical Device Products as Medical Devices: Learning from the Case of PARO
    • Funding, Partnering & Networking >
      • Utilization of Public Grants and Subsidies
      • J-Ships
    • Intellectual Property >
      • patent or trade secret?
      • employee invention
      • Matching of Patents Held by Startups and Individuals
    • Legal & Contracts >
      • References for Contracts
      • Guide to Industry-Academia Collaboration Agreements for Academic Researchers
    • Academia & Tech Transfer
    • Licensing, partnering >
      • Networking, Partnering
      • Introducing Seeds to Pharmaceutical Companies
      • Incentives (Returns) to Licensor Universities
    • References in English
  • コンテンツ一覧
    • 起業、法人設立・運営 >
      • 事業計画の策定
      • 法人設立
      • ライフサイエンスハブ、スタートアップハブ
    • 公的支援 >
      • 公的支援機関リスト
      • 大学発スタートアップ支援機関・プログラムガイド
      • AMED Medical IP Desk
      • MEDISO活用のススメ
    • 薬事・規制関連 >
      • PMDA RS相談活用のススメ
      • 薬事スタッフ・コンサル選定ガイド
      • 都道府県薬務課一覧
      • コンビネーション製品、組合せ医療機器、キット製品、組合せ医薬品
    • 医薬品、再生医療等製品 >
      • 医薬品の該当性確認方法
      • 医薬品一般的名称設定のガイドライン
      • 医薬品、医療機器等の開発に当たって、参照したい資料
      • 先進医療制度
      • 一般用医薬品(OTC)
      • コンパニオン診断薬と遺伝子パネル検査
      • 再生医療等製品の保険償還(原価計算)に関する参考情報
    • 医療機器、体外診断用医薬品 >
      • 体外診、ラボ開発検査、研究用試薬
      • 医療機器該当性確認ガイド
      • 医療機器と非医療機器の機能が複合した製品は?
      • 医療機器の一般的名称と確認方法
      • 医療機器のクラス分類
      • 医療機器・体外診の保険収載
      • SaMDの保険収載
    • ヘルスケア・ケアテック >
      • 非医療分野の検査サービスを展開する際に注意すべきポイント
      • 治療用装具と補装具
      • 化粧品及び医薬部外品
      • 医療機器とするか、非医療機器とするか
    • 資金調達 >
      • 公的な助成金、補助金の活用
      • 特定投資家向け銘柄制度(J-Ships)
      • アカデミア研究者がPIとして応募可能なグラントリスト
      • 海外在住の日本人研究者が日本の助成金を獲得する方法
    • 知的財産 >
      • 特許か?営業秘密か?
      • 職務発明:アカデミア・公的研究機関に所属する研究者が注意すべきポ
      • スタートアップや個人が保有する特許のマッチング
      • ライセンスを受けた大学へのインセンティブ(還元)について
    • 法務・契約 >
      • 契約関連で参考になる公的機関の資料
      • 個人情報を利用する製品開発時の 留意すべき法規制
    • アカデミア、技術移転 >
      • アカデミア研究者のための産学連携契約ガイド
    • ライセンシング、パートナリング >
      • 製薬企業等へのシーズ紹介
      • ネットワーキング、パートナリング
    • 海外展開 >
      • 米国展開(主に医療機器)に、読むと役立つ情報リスト
      • 米国FDAにおける、医療機器該当性の確認ステップ
      • 米国における、医療機器の申請データ・試験計画の相談方法((Pre-Submission/Q-Submission
      • 公的機関の海外展開支援
      • 横浜市の公的支援サービス
      • JETROを徹底活用しよう
      • 日米欧での医療機器定義の比較
      • 簡略審査(審査の迅速化)
      • 海外規制等の情報収集
      • 非医療機器製品の海外での医療機器展開
      • 欧州医療機器規則MDRに関する資料
      • 欧州MDRにおける、医療機器該当性の確認方法
    • オーストラリア >
      • オーストラリア研究開発優遇税制の概要
      • オーストラリア研究開発優遇税制の適用を受けるには
      • オーストラリアでの主要イベント
      • R&D関連の公的機関
      • オーストラリア助成金情報