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EXHIBIT 10.7 AMENDED AND RESTATED DISTRIBUTION AGREEMENT

Distribution Agreement

EXHIBIT 10.7    AMENDED AND RESTATED DISTRIBUTION AGREEMENT | Document Parties: HEMOSENSE INC | Quality Assured Services, Inc. You are currently viewing:
This Distribution Agreement involves

HEMOSENSE INC | Quality Assured Services, Inc.

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Title: EXHIBIT 10.7 AMENDED AND RESTATED DISTRIBUTION AGREEMENT
Governing Law: Florida     Date: 3/31/2005

EXHIBIT 10.7    AMENDED AND RESTATED DISTRIBUTION AGREEMENT, Parties: hemosense inc , quality assured services  inc.
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E XHIBIT 10.7

 

AMENDED AND RESTATED DISTRIBUTION AGREEMENT

 

This AGREEMENT is made as of March 1 st 2005 (the “ Effective Date ”), by and between HemoSense, Inc., (hereafter referred to as “ HemoSense ”), a California Corporation, and Quality Assured Services, Inc. (aka, QAS), with its principal place of business 1506 N Orange Blossom Trail, Orlando, Florida, 32804 (hereafter referred to as “ Distributor ”). As used in this Agreement, HemoSense and Distributor are each referred to as a “ Party ” and collectively as “the Parties .” This Agreement amends, supercedes and restates in its entirety the Distribution Agreement by and between the Parties dated March 31, 2003 (the “ Original Agreement ”).

 

WITNESSETH:

 

WHEREAS HemoSense manufactures products, which include instrumentation and reagents designed for testing various blood analytes.

 

WHEREAS, Distributor desires to distribute and market the devices and related test supplies subject to the conditions set forth herein.

 

NOW, THEREFORE, in consideration of the premises hereof and the mutual covenants and conditions hereinafter set forth and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereto, intending to be legally bound, hereby agree as follows:

 

ARTICLE 1 – APPOINTMENT

 

HemoSense hereby appoints Distributor and Distributor hereby accepts appointment as a non-exclusive distributor of the HemoSense products listed or described on Exhibit A (the “ Products ”), commencing on the date that the Original Agreement was executed by both Parties.

 

When new products as part of the product line become available, HemoSense will notify Distributor and Distributor will have the right to purchase these new products from HemoSense under the terms of this Agreement.

 

ARTICLE 2 – TERMS OF AGREEMENT

 

2.1

The initial term of this Agreement commences upon the Effective Date and ends February 28, 2007 (the “ Initial Term ”). Upon the expiration of the Initial Term, and each Renewal Term thereafter (if any), this Agreement shall be automatically renewed for a one-year term (each, a “ Renewal Term ”) unless terminated by either Party in writing and in accordance to Article 19 of the Agreement.

 


***

Confidential treatment requested pursuant to a request for confidential treatment filed with the Securities and Exchange Commission. Omitted portions have been filed separately with the Commission.

 

Page 1 of 15


2.2

No modification of this Agreement is effective or binding unless in writing and signed by the Parties. This Agreement consists of thirteen (13) pages, including exhibits.

 

2.3

Distributor’s authority under this Agreement is limited to directly distributing the Products solely to the end-user customers within the markets and channels identified on Exhibit B (the “ Permitted Markets/Channels ”) solely in the territory identified on Exhibit B (the “ Territory ”).

 

2.4

DISTRIBUTOR has no authority or right, either legal or apparent, expressed or implied, to bind HemoSense in any contractual, financial, or legal obligation.

 

2.5

Both Parties agree to hold harmless and indemnify the other for any loss or damage sustained by the other as a direct result of their malfeasance or action which exceed their rights or authority in this Agreement.

 

ARTICLE 3 – OBLIGATIONS OF THE DISTRIBUTOR

 

3.1

The Distributor will develop adequate numbers of suitably qualified personnel as well as suitable equipment and infrastructure for efficient warehousing, distribution and sale, and other services related to the Products throughout the Territory.

 

3.2

The Distributor will provide appropriate and professional installation and application advice (within [***] business days of delivery to its customers), follow-up services and advice, 24-hour on-call support, insurance reimbursement services, regulatory requirements advice and guidance, technical support, training/help/support and, at their option, data management programs to purchasers of Products when so requested by the purchaser at no charge to HemoSense.

 

3.4

The Distributor will inform HemoSense on a timely basis of any claims, complaints, adverse events or deficiencies concerning the Products in the Territory and shall provide reasonable assistance to HemoSense in handling such claims and events within a 48 hour period

 

3.5

The Distributor will maintain stocks of all the Products at an appropriate level determined by HemoSense and Distributor having regard to the monthly sales thereof in the Territory and will ship product to purchasers the same business day it is requested, when orders are received by 3:00 p.m. EST on normal business days.

 

3.6

Within three weeks of the Effective Date, the Distributor will provide HemoSense with its unit per month Product sales forecast for the six (6) month period commencing with the first day of the month following the Effective Date (the “ Initial Forecast ”). The Initial Forecast will be categorically itemized by the

 


***

Confidential treatment requested pursuant to a request for confidential treatment filed with the Securities and Exchange Commission. Omitted portions have been filed separately with the Commission.

 

Page 2 of 15


 

various components of the Product, (i.e. projected monthly purchases of meters, strips and other INRatio disposables). By the first ( 1 st ) day of the month after the Effective Date, and on the 1 st day of each month thereafter, the Distributor will provide updated twelve (6) month rolling forecasts (the “ Rolling Forecast ”).

 

3.7

Distributor shall, at its own expense, and in a manner consistent with the sales policies of HemoSense:

 

 

(a)

place the Product in Distributor’s catalogues as soon as possible, attend such the appropriate trade shows and display the Product in any applicable trade show that it attends;

 

 

(b)

provide adequate contact with existing and potential customers within the Permitted Markets/Channels and Territory on a regular basis, consistent with good business practice;

 

 

(c)

assist HemoSense in assessing customers’ requirements for the Product, including modifications and improvements thereto, in terms of quality, design, functional capability, and other features; and

 

 

(d)

submit market research information, as reasonably requested by HemoSense, regarding competition and changes in the market within the Territory.

 

3.8

If requested by HemoSense, Distributor shall develop an annual business plan for the Product which shall include, without limitation, promotion strategy and tactics, and sales and other marketing plans (“ Business Plan ”). Any such Business Plan shall be provided to HemoSense for prior review and approval, which approval shall not be unreasonably withheld. The Business Plan for the first year of this Agreement shall be provided to HemoSense within one (1) month after the Effective Date, and no request therefore need be made by HemoSense. Thereafter, if requested, Distributor shall provide Business Plans to HemoSense for review and approval not later than sixty (60) days before January 1 of the Calendar Year to which such Business Plan pertains.

 

ARTICLE 4 – OBLIGATIONS OF THE COMPANY

 

4.1

HemoSense will use commercially reasonable efforts to maintain stocks of all the Products at an appropriate level having regard to the monthly sales thereof in the Territory. HemoSense will inform the Distributor of the available stock of the Products and will provide the Distributor feedback on product deliveries (e.g. order confirmation including availability of product and shipping schedules within 24 hours of receipt of the order).

 

4.2

HemoSense will use good faith commercial efforts to process and ship all orders in accordance with requested delivery dates subject to availability and mutual agreement on delivery dates. However, no Distributor purchase orders for Products are binding on HemoSense unless accepted by HemoSense in writing.

 


***

Confidential treatment requested pursuant to a request for confidential treatment filed with the Securities and Exchange Commission. Omitted portions have been filed separately with the Commission.

 

Page 3 of 15


4.3

The delivery date requested in a Distributor purchase order shall be considered the date Distributor requests shipment by HemoSense. HemoSense will determine, in its sole discretion, the shipping origin of the Product. The shipping confirmation will be provided to the Distributor by fax and/or by e-mail. Products shipped by HemoSense under this Agreement will, at the time of shipment, have a remaining shelf life of at least [***] ([***]) months.

 

4.4

HemoSense will provide to the Distributor reasonable Product support and marketing support including training in demonstration and use of the Products. HemoSense will also supply the Distributor with price lists, literature and support materials, advertising and support of sales programs, as well as after sales service and technical support. HemoSense will establish a [***] that will be funded by [***]% of gross product sales from HemoSense to Distributor. These funds will be utilized exclusively on marketing programs specifically for Distributor. For purposes of this Section 4.4, “Target Sales” means, for each calendar year during the term of this Agreement, the following:

 

 

 

 

Calendar Year


 

  

Target Sales


 

2005

  

$[***]

 

 

2006

  

$[***]

 

 

2007 (and each

calendar year thereafter)

  

As determined by agreement of the Parties, as necessary to provide appropriate incentives for increase sales

 

In addition, within sixty (60) days after the end of each calendar year during the term of this Agreement, HemoSense will determine if the gross product sales from HemoSense to Distributor exceeded the Target Sales for such calendar year. Where such Target Sales were exceeded, HemoSense will add to the [***] an additional amount equal to [***] percent ([***]%) of the overall gross product sales from HemoSense to Distributor in the just-completed calendar year. If at such time (that is, within sixty (60) days after the end of each calendar year during the term of this Agreement) the marketing co-op fund includes a surplus funding balance that HemoSense has not utilized, and does not reasonably anticipate utilizing, on marketing programs specifically for Distributor as contemplated under this Section 4.4, HemoSense will issue a credit to Distributor for the surplus amount.

 


***

Confidential treatment requested pursuant to a request for confidential treatment filed with the Securities and Exchange Commission. Omitted portions have been filed separately with the Commission.

 

Page 4 of 15


ARTICLE 5 – RECORD KEEPING

 

The Distributor shall track and record a reasonable level of traceable detail of product sold to the Distributor’s customers under this Agreement. These records will include, but not be limited to customer name, address, Product # detail, price, lot number (for reagents) and serial number (for instruments). Distributor agrees to maintain these records during the term of the Agreement. These records will include monthly sales tracing reports by Product, Product number, sales, and/or account or zip code that will be sent to HemoSense no later then 30 days from the end of a calendar month. These tracings are to be used to provide commission and sales reporting to the HemoSense sales force.

 

The Parties agree to meet no less than twice yearly for half to full-day reviews of their mutual business. These reviews will be conducted in alternating locations (i.e. alternating between Distributor’s offices and HemoSense’s offices).

 

ARTICLE 6 – CONFIDENTIALITY

 

For the purposes of this Article 6, the term “Confidential Information” shall be any information embodying a whole or any portion or phase of any business, scientific or technical information, design, process, procedure, formula, improvement, concept, idea, technique, know-how, market data, and accounting data which both:

 

 

(a)

is disclosed by one Party hereto to the other; and

 

 

(b)

is secret, confidential, and proprietary to the disclosing Party at the time of disclosure and is marked as such

 

During the period this Agreement remains in effect and for a period of five (5) years following termination thereof, each Party (except as is explicitly otherwise required, permitted or consistent with the terms hereby) shall keep confidential, shall not use for itself or the benefit of others, and shall not copy or allow to be copied, in whole or in part, any Confidential Information disclosed to such Party by the other.

 

The obligations of confidentiality imposed upon the Parties by the foregoing Paragraph


 
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