Most of my career has been meeting customers across the globe. Some rules that I followed which helped me build great rapport with them

Keep business away from personal time. Most of the times while visiting them, my clients take me out for dinner post meeting. Avoid talking business during meals. Even if you’re at a business lunch, don’t start talking shop until you’re done with the dessert.
When meeting or pitching to clients, people tend to make the mistake of talking about how much the customer is going to benefit, while avoiding the subject of what they’ll get out of the deal. Be transparent and upfront about how both the client, and yourself, will benefit.
If you make a mistake, like we did recently by shipping a wrong product,be apologetic and go the extra mile by making a gesture of goodwill free shipping on their next order.This way,you’re likely to keep the customer,who may even spread the word about how great your service is.
Do some homework about what the company is doing new by researching about them online - like a new product they are developing or a new plant they are setting up. Gives a good topic to discuss during breaks.

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@franciscodeasis https://t.co/OuQaBRFPu7
Unfortunately the "This work includes the identification of viral sequences in bat samples, and has resulted in the isolation of three bat SARS-related coronaviruses that are now used as reagents to test therapeutics and vaccines." were BEFORE the


chimeric infectious clone grants were there.https://t.co/DAArwFkz6v is in 2017, Rs4231.
https://t.co/UgXygDjYbW is in 2016, RsSHC014 and RsWIV16.
https://t.co/krO69CsJ94 is in 2013, RsWIV1. notice that this is before the beginning of the project

starting in 2016. Also remember that they told about only 3 isolates/live viruses. RsSHC014 is a live infectious clone that is just as alive as those other "Isolates".

P.D. somehow is able to use funds that he have yet recieved yet, and send results and sequences from late 2019 back in time into 2015,2013 and 2016!

https://t.co/4wC7k1Lh54 Ref 3: Why ALL your pangolin samples were PCR negative? to avoid deep sequencing and accidentally reveal Paguma Larvata and Oryctolagus Cuniculus?

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