طريقة التسجيل كبائع في مرسالي؟

مرحبا بك في مجتمعنا!

كل ما عليك فعله لتبدأ ببيع الهدايا في “مرسالي” هو اتباع الخطوات الآتية:

1- قم بفتح صفحة (التسجيل/تسجيل الدخول) على موقعنا، 

2- قم بإدخال المعلومات اللازمة للتسجيل كمستخدم جديد تحت قسم (تسجيل جديد)،

3- حدد خيار (أنا بائع) ثم اضغط على زر (تسجيل جديد).

انتظر فقط بعض الوقت حتى يقوم المسؤول بالموافقة على طلبك للتسجيل كبائع في مرسالي ..

 بمجرد الموافقة على طلبك، تستطيع فورا البدء بعرض منتجاتك و نشرها للعامة في مجتمع “مرسالي”. هنيئا لك! 

أنت الآن بائع هدايا في مرسالي وجزء من عائلتنا..

نود الآن تنبيهك إلى أمر مهم حتى تستطيع نشر منتجاتك بطريقة احترافية على الموقع لتحقق مبيعات أكثر،

 فكلما اتبعت الخطوات التي سنرشدك من خلالها و التزمت بها أكثر ستجد مبيعاتك تفوق تصوراتك وستتفوق على منافسيك من البائعين الآخرين على موقعنا!

قم بمشاهدة الفيديوهات التعليمية لإرشادك حول إدارة حسابك كبائع باحترافية، و كذلك طريقة نشر منتجاتك على الموقع بطريقة صحيحة و غيرها من الأمور المهمة لك كبائع في مرسالي.

52٬117 فكرة عن “طريقة التسجيل كبائع في مرسالي؟”

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    A formula of oro-dispersible tablet computers (ODT) is swiftly dispersed in the mouth and can be administered without water, making it highly useful in people with swallowing conditions. Vardenafil ODT was first authorized to treat ED by the Food and Drug Administration in 2010 [63] However, though the ODT formula of vardenafil increases bioavailability, the healing impacts and adverse events were not enhanced compared to those of vardenafil film-coated tablet computers (FCT). A phase I professional test took a look at the pharmacokinetics of sildenafil ODT in 36 healthy and balanced topics. Sildenafil ODT had a comparable pharmacokinetic account as the FCT form, and high fat meals minimized the price of absorption of sildenafil contrasted to the film-coated kind.

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    A well-documented pro-erectile pathway entails the abovementioned OT neurons estimates from the paraventricular core to the sacral parasympathetic cores expressing the OT receptors. Despite many dissatisfactions, a number of prominent therapeutic targets have caught the focus of the clinical community34,164,165,166 (Table 2). They show the state-of-the-art in exactly how unique medication prospects have been identified and advanced to human study.
    This renovation of the ARCAgRP/NPY forecasts correlates with enhanced activation of paraventricular hypothalamic cores nerve cells with the objective to restore food intake114. An additional barrier in weight-loss pharmacology is that persistent elevation of adiposity signals such as leptin and insulin cause desensitization, bring about an impaired responsiveness of this homeostatic system115,116,117. A striking finding sustaining this viewpoint is that leptin supplementation shows amazing efficacy in decreasing body weight in people with congenital leptin deficiency96,118,119, however is largely inefficient in even more common polygenetic forms of obesity115,116,117. Although estrogenic-EDC exposure throughout development and their adult years has unhealthy results on erectile feature, endogenous estrogen likewise has a duty in penis advancement which might advertise erectile feature in the grownup. Computer mice with disrupted endogenous estrogen signalling show accelerated delamination of the penis tissues, influencing the timing of the separation of the prepuce from the glans [Cripps et al., 2019; Govers et al., 2019]
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