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LICENSING AND DISTRIBUTION AGREEMENT

Distribution Agreement

LICENSING AND DISTRIBUTION AGREEMENT You are currently viewing:
This Distribution Agreement involves

AURIGA LABORATORIES, INC.

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Title: LICENSING AND DISTRIBUTION AGREEMENT
Governing Law: Delaware     Date: 10/19/2007
Industry: BIOTRX     Sector: Healthcare

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LICENSING AND DISTRIBUTION AGREEMENT  


Agreement made this 6 th   day of June, 2007, between Laboratoires Carilène S.A.S a corporation existing under the laws of France, and having its principal place of business at 7, rue du Chant des Oiseaux, 78360 Montesson-France (hereinafter referred to as “Supplier”), and Auriga Laboratories, Inc., existing under the laws of the State of Delaware, U.S.A, having its principal place of business at 2029 Century Park East, Suite 1130, Los Angeles, CA 90067 U.S.A. (hereinafter referred to as “Buyer”).

WITNESSETH :

WHEREAS, The Supplier desires to sell and the Buyer desires to buy the Product defined below and described in Exhibit C hereto; and

WHEREAS, The   Supplier is willing to furnish all of Buyer’s requirements for the Product and Buyer is willing to purchase all of its requirements for the Product from Supplier, subject to Supplier’s ability to meet Buyer’s demand for the Product; and

WHEREAS, The Buyer shall be the exclusive distributor of the Product in the Territory. Supplier is the exclusive owner of an invention relating to the use in treatment for alopecia and the subject of United States Patent No. 6,001,378 and subject to a PCT filing number PCT/FR97/00141 filed January 24, 1997, as listed in Exhibit D attached hereto, and all claims therein, that covers the Product (hereinafter called the “Invention’); and

WHEREAS, The   Supplier will transfer to the Buyer the Information, as well as scientific and marketing data which are essential to the manufacture and commercial exploitation of the Product.

NOW THEREFORE, this Agreement witnesses that for and in consideration of the respective covenants and agreements herein contained, it is agreed by and between the parties as follows:
 

ARTICLE 1
DEFINITIONS


1.1.
Definitions. For the purpose of this Agreement or any amendment thereto, the following terms shall have the following meanings, respectively :

1.1.1. “Product(s)” shall mean combinations, in particular for use as the active principle in a cosmetic and particularly dermatological composition, containing peroxidised lipids and organosilicon compounds containing them, as well as their applications, including but not limited to the combination known in Europe as “Silicium 44 Lotion” and “Silicium 44 Shampoo” as covered by the Patent and all other Supplier intellectual property rights and as further described in Exhibit C and covered by the Patent listed in Exhibit D. Product shall include all successor products and all line extensions, upgrades, new formulations and the like. Product shall also include sample packages as mutually agreed to between the parties from time to time.

1.1.2. “Territory” shall mean the United States of America and its possessions and territories

1.1.3. “Information” shall mean all trade secrets, data, information and know-how related to the Invention, Product and the Patent.



1.1.4. “Patent” means the U.S.A. Patent No. 6,001,378, as described above and further described in Exhibit D, including all divisionals, reissuances, reexaminations, foreign counterparts and the like.

1.1.5 Transfer price shall mean the price in EURO, paid by the Buyer to Supplier for the Product as described below in Article 5.4

1.1.6 “FCA” shall have the meaning ascribed thereto in INCOTERMS 2000 of the International Chamber of Commerce, meaning, among other things, that Supplier shall deliver the goods cleared for export, at Supplier’s expense, and Buyer shall clear, at its expense, the goods for import into the Territory.

1.1.7 “Quality Assurance Agreement”: The Quality Assurance Agreement shall ensure all applicable governing laws, rules and regulations including but not limited to those relating to Good Manufacturing Practices (GMPs) and under the European guide line of registration of Cosmetic file (see appendix).

1.1.8 “Manufacturing Package” means all Information and instructions necessary to enable a third party to manufacture the Product if permitted pursuant to this Agreement.

1.1.9 “Net Sales” means all amounts actually received by the Buyer as a results of its sales of Products less all the deductions for discounts, products
Rebates, forces or mandated wholesales/distributors fees, rebates to other government agencies or purchasing associations, returns, charges back and imported fess. These rebates cannot exceed 15% of gross sales.
 

ARTICLE 2
REQUIREMENTS AND EXCLUSIVITY


2.1. License. Except as otherwise explicitly provided for in this Article 2, Supplier hereby grants to Buyer the exclusive (even as to Supplier) right, under all applicable worldwide intellectual property rights, to sell, market, distribute, sublicense and exploit the Product in the Territory under The trade name of Silicium 44 (Lotion and Shampoo). Except as otherwise explicitly provided for in this Article 2, Buyer is also hereby granted an exclusive right and license, under all applicable worldwide proprietary rights, to make, have made, use, sell, have sold, market, distribute, sublicense and manufacture the Product, but only if and when expressly authorized under the terms and conditions of this Agreement.

2.2   Sale of Requirements . During the term of this Agreement, Supplier agrees to sell to Buyer all of Buyer’s requirements of the Product in accordance with the terms of this Agreement. If Supplier is unable to supply all of Buyer’s requirements, Supplier shall, as Buyer’s sole remedy, use commercially reasonable efforts to provide Buyer, at prices at or lower than those set forth in this Agreement, with the Product from other sources to avoid out-of-stock situations. Notwithstanding the foregoing, if Supplier is unable to supply Buyer’s requirements two (2) or more times during a ninety (90) day period, then Buyer shall have the right to require qualification of a second manufacturer, of Buyer’s choice, to manufacture the Product for Buyer by using the Manufacturing Package. Such additional manufacturer shall be subject to the confidentiality restrictions set forth herein.

2.2.1 Purchase of Requirements . During the term of this Agreement, Buyer agrees to buy from Supplier all of Buyer’s requirements for the Product in accordance with the terms of this Agreement.





2.3 . Exclusivity . During the term of this Agreement, except with respect to, Supplier agrees not to distribute or sell the Product directly or indirectly to any other party for the purpose of use or sale in the Territory in accordance with Article 2.1. If during the Term of the Agreement, Buyer at any time notifies Supplier that a party is distributing or selling Product in the Territory Supplier agrees that it will take all action necessary to immediately halt all sales (direct and indirect) of Product to such party that is distributing or selling in the Territory providing that the source of the product is identified to be the Supplier. In the event any damages are recovered as a result of Supplier’s actions, after reimbursing Supplier its reasonable costs to take such action, all remaining proceeds shall belong to Buyer, subject to the royalty set forth in Article 5.3 If the source of the Product is other than Supplier, then Buyer shall have the right, by virtue of the exclusive license granted in Article 2.1, to take action against such third party, and all proceeds of any such action shall belong solely to Buyer, subject to the royalty set forth in Article 5.3.
 
2.4. No Sales Outside the Territory . Buyer shall not, without the prior written approval of Supplier (to be granted or withheld in Supplier’s sole and absolute discretion), directly or indirectly sell Product outside the Territory, advertise, promote or solicit customers for Product outside the Territory, establish any office outside the Territory through which orders are solicited or establish any depot at which inventories of Product are stored outside the Territory.

2.5   Right of First Refusal . In the event Supplier decides to grant an exclusive right to distribute and sell any further Supplier products in the Territory, and such products are not included under the definition of Products set forth in this Agreement, Supplier shall provide Buyer the first opportunity to obtain such exclusive right for such products upon mutually agreed upon terms and conditions. Upon receiving information regarding new Products, Buyers shall have 90 days to exercise right of first refusal.
 

ARTICLE 3
REPRESENTATIONS


3.1. Representations of Supplier . The Supplier represents that:

3.1.1. Supplier is the exclusive owner of all rights, title and interest in and to the Invention, Patent, and Information, and has the right to grant to Buyer the rights and licenses set forth in this Agreement. The Invention and Products are completely safe for human use and does not have any direct or indirect adverse health effects.

3.1.2. As of the date of this Agreement, other than the Patent, Supplier has not filed, or caused to be filed in the U.S., patent applications, or obtained in its name or caused to obtain in the name of others, any other patent based on or relating to the Invention, Information or devices or methods similar to the Invention.

3.1.3. Supplier has, and will continue to, comply with all applicable laws, rules and regulations with respect to the development, manufacture, sale, use and distribution of the Product (“Laws”).

3.2. Information . Supplier shall furnish to Buyer, or its nominees, any Information reasonably required (as determined by Supplier and Buyer) by Buyer to commercialise and exploit the use of the Invention and the Products permitted under this Agreement, including without limitation the clinical data and related materials that were conducted on the Invention and/or Products.




3.3. Buyer represents that Buyer (i) will adhere to all applicable laws, rules and regulations, relating to the sale of Product in the Territory; and (ii) will store the Product in appropriate conditions and facilities (as instructed by Supplier).
 

ARTICLE 4
GENERAL OBLIGATIONS  


4.1. Buyer’s Obligations . Marketing and distribution . In addition to any and all other obligations and liabilities of Buyer as provided in this Agreement, Buyer or Buyers successors shall use commercially reasonable efforts to promote and market the Product for sale according to the business plan covering the first 3 years communicated to Supplier.

4.2   Supplier’s Obligations.

4.2.1. Lead time : Lead time for Products ordered hereunder shall be 16 weeks for the first order after reception of the final art work data signed by both supplier and buyer, and then 16 weeks after receipt of all other orders. Shipment time by ocean shall be 4/5 weeks; by air-freight shall be 1 week. Shipment time shall be added to lead time for purposes of scheduling delivery. 50% of total billing for the first order only, will be paid by money bank transfer at order time.

4.2.2. Supplier shall provide Buyer with a Certificate of Analysis for batches of Product by facsimile three (3) working days prior to shipment. Original copies of the Certificates of Analysis shall be sent regular mail.

4.2.3. Supplier shall provide Buyer with a copy of the bill of lading by facsimile upon shipment.

4.3   Manufacturing Rights . In the event Supplier admits in writing its inability to pay its debts generally as they become due, files an assignment or a petition in bankruptcy, as the case may be, or a petition to take advantage of any insolvency statute, makes a general assignment for the benefit of its creditors, consents to the appointment of a receiver of itself or of the whole or any substantial part of its property, undertakes its liquidation, winding-up or dissolution, or enters into an arrangement or composition with or for the benefit or creditors generally occurring in circumstances in which it is unable to meet its obligations as they fall due, then Buyer shall have a non-exclusive right and license to use the Manufacturing Package and to select a third party to manufacture the Product for continued distribution in the Territory. In the event Buyer exercises its rights under this Section 4.3, all royalties payable hereunder shall remain unchanged. Supplier shall place the Manufacturing Package in escrow pursuant to a mutually agreed upon escrow agreement that enables release of the Manufacturing Package upon written notice of the occurrence of any of the foregoing release conditions. When Supplier recovers it’s total ability to run it’s business normally, the Buyer’s manufacturing rights under this Section 4.3 shall terminate and the provisions, terms and conditions of this Agreement shall be in full force and effect.
 

ARTICLE 5
PRICE AND TERMS


5.1. Payments : In consideration of the exclusive license granted in Article 2.1, upon receipt of Product pursuant to orders by Buyer, Buyer shall pay to Supplier a non refundable premium of USD $1.5 million in accordance with the following payment schedule:
(i) US$ 250 000 upon the commercial launch of the product in the US



(ii) US$ 500 000 on or before the 90 th day after commercial launch of the product in the US
(iii) US$ 750 000 upon the earlier twelve month after the commercial launch of the Product or at the time that Buyer achieves £ 5 000 000 of net Sales in the first year.

5.2 The transfer price of the two presentations, SILICIUM (Lotion & Shampoo) are defined as below and calculated in a USA$ with a fix exchange rate as specified in the article 5.4

(i).   EURO 3.80 per bottle of Silicium 44 Lotion,
(ii).   EURO 2.80 per bottle of Silicium 44 Shampoo.

Buyer shall pay these amounts to Supplier in US Dollars at the then existing Transfer Price as calculated in Section 5.4.

5.2. Minimum Batch size : The minimum batch size for   stock bottles of either the Silicium 44 Lotion or Silicum 44 Shampoo shall be 50,000 units per product.

5.3 Royalties: Buyer will pay royalties equal to five per

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